Genetic distance measures how close you are to a given sample.
10 means this is your ancient ancestry
20 means this is part of your ancestral link
30 means possibly related to your ancestry
Your DNA matches these ancient populations based on real archaeological samples from over 150 Ancient Civilizations. Touch the buttons below to learn more about them.
Phoenician + Carthaginian (6.553)
Sicani + Phoenician (6.641)
Roman Hispania + Phoenician (6.924)
Dacian + Phoenician (6.934)
Roman Hispania + Sicani (8.622)
Phoenician (9.36)
Carthaginian (13.1)
Sicani (13.28)
Roman Hispania (13.84)
Dacian (13.86)
Your closest genetic modern populations..
1. Spanish_Andalucia (16.10)
2. Spanish_Aragon (17.13)
3. Spanish_Castilla_La_Mancha (17.62)
4. Spanish_Valencia (17.72)
5. Spanish_Cantabria (19.47)
6. Southwest_French (19.75)
7. Spanish_Murcia (19.85)
8. Spanish_Extremadura (20.14)
Ancient Sample Breakdown:
1. Palestinian (8.337)
2. Samaritian (9.216)
3. Coptic_Egyptian (10.21)
4. Egyptian (10.53)
5. Jordanian (10.80)
6. Libyan_Jewish (12.25)
7. Tunisian_Jewish (13.48)
8. Bedouin (14.32)
Late Period Ancient Egypt 650 BC
JK2911
mtDNA: M1a1Y-DNA: J2b1 (M205)Shared DNA: (Sample Quality: 5)
4 SNP chains (min. 60 SNPs) / 421.16 cM
Largest chain: 17392 SNPs / 120.24 cM
Your raw DNA is 100 % closer than other matching users
Chr. 1 17392 SNPs
Chr. 2 17058 SNPs
Chr. 3 13834 SNPs
Chr. 4 11521 SNPs
Your raw DNA is 100 % closer than other matching users
JK2911
mtDNA: M1a1Y-DNA: J2b1 (M205)Shared DNA: (Sample Quality: 5)
4 SNP chains (min. 60 SNPs) / 421.16 cM
Largest chain: 17392 SNPs / 120.24 cM
Your raw DNA is 100 % closer than other matching users
Chr. 1 17392 SNPs
Chr. 2 17058 SNPs
Chr. 3 13834 SNPs
Chr. 4 11521 SNPs
Your raw DNA is 100 % closer than other matching users
How many SNPs is a good match?
Finding genetic relatives
Our simulations have concluded that we can confidently detect related individuals if they have at least one continuous region of matching SNPs (Single Nucleotide Polymorphisms) that is longer than our minimum threshold of 7cM (centiMorgans) long and at least 700 SNPs.
Ah, let us delve into the fascinating life and times of an individual from Late Period Ancient Egypt, who walked the banks of the Nile some 2,650 years ago. His genetic lineage whispers tales of bygone eras, with paternal ancestry rooted in the Y-DNA Haplogroup J2b1, indicating connections that may trace back to the Fertile Crescent. This bears witness to the ancient movements of peoples, as Mediterranean cultures intertwined with those of Egypt. On his mother's side, the MTDNA Haplogroup M1a1 presents a tapestry of maternal heritage, possibly originating from eastern Africa or the Near East, enriching our understanding of the genetic melting pot that was the Nile Valley.
Wrapped in the embrace of the sand for untold centuries, the mans remains offer a gateway into the customs and daily life of his time. Late Period Egypt was a time of both turmoil and opulence, as the nation grappled with the pressures of foreign influences and internal changes. This period was marked by artistic and religious revivals as well as political fragmentation, which sometimes led to foreign rule by powers such as the Assyrians and Persians before the eventual conquest by Alexander the Great.
65.4%
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Dark Ages Italy South Tyrol Malles Burgusio Santo Stefano | 450 AD (2418) | Genetic Distance: 14.96 | mtDNA: H | ||
Dark Ages Italy South Tyrol Malles Burgusio Santo Stefano | 450 AD (2420) | Genetic Distance: 20.23 | mtDNA: K1a4 | ||
Dark Ages Italy South Tyrol Malles Burgusio Santo Stefano | 450 AD (2425) | Genetic Distance: 19.1 | mtDNA: H1e | Y-DNA: E1b1b1a1b1a | |
Dark Ages Italy South Tyrol Malles Burgusio Santo Stefano | 450 AD (2426) | Genetic Distance: 18.01 | mtDNA: H1q | Y-DNA: R1a | |
Gallic Cenomani Tribe Italy Verona Seminario Vescovile | 300 BC (3220) | Genetic Distance: 17.85 | mtDNA: X2b6 | Y-DNA: R1b1a1b1a1a2b1 | |
Gallic Cenomani Tribe Dog Co-Burial Italy Verona Seminario Vescovile | 300 BC (3227) | Genetic Distance: 21.12 | mtDNA: U5b3 | Y-DNA: R1b1a1b1a2a1 | |
Gallic Cenomani Tribe Horse Co-Burial Italy Verona Seminario Vescovile | 300 BC (3265) | Genetic Distance: 19.65 | mtDNA: H4a1c1a | ||
Gallo-Celtic Switzerland Pont de Cornaux-Les-Sauges | 200 BC (3437) | Genetic Distance: 17.34 | mtDNA: HV | Y-DNA: E1b1b1a1b1a10a1a1b | |
Deep Dive Late Period Ancient Egypt | 650 BC (JK2911) | Total shared SNPs: 59805.0 | Largest SNP chain: 17392.0 | mtDNA: M1a1 | Y-DNA: J2b1 |
Deep Dive Carthago-Iberian-Mehrebi Cordoba Caliphate | 950 AD (I7500) | Total shared SNPs: 122.0 | Largest SNP chain: 122.0 | mtDNA: M1b1a | Y-DNA: E1b1b1b1a1 |
Deep Dive Iron Age Forest Steppes Ukraine Poltava Chernyakhiv | 229 AD (UKR121) | Total shared SNPs: 113.0 | Largest SNP chain: 113.0 | mtDNA: H1 | |
Deep Dive Late Roman Era Bulgaria Boyanovo | 400 AD (I18792) | Total shared SNPs: 106.0 | Largest SNP chain: 106.0 | mtDNA: H14b | Y-DNA: E1b1b1a1b1 |
Deep Dive Carthaginian Roman-Era Empuries | 200 BC (I8204) | Total shared SNPs: 104.0 | Largest SNP chain: 104.0 | mtDNA: H1e | |
Deep Dive Ptolemaic Egypt | 50 BC (JK2888) | Total shared SNPs: 129.0 | Largest SNP chain: 129.0 | mtDNA: U6a2 | Y-DNA: E1b1b1a1b2-V22 |
Deep Dive Carthaginian Sardinia Villamar | 250 BC (VIL011) | Total shared SNPs: 135.0 | Largest SNP chain: 135.0 | mtDNA: K1a3a | Y-DNA: R1b1a1b1a2 |
Deep Dive Late Roman Empire Viminacium Serbia Grobalja Necropolis | 250 AD (I15518) | Total shared SNPs: 214.0 | Largest SNP chain: 112.0 | mtDNA: U2e1a1 | Y-DNA: E1b1b1a1b1a |
Deep Dive Early Bronze Age Bulgaria Yunatsite | 3120 BC (YUN045) | Total shared SNPs: 135.0 | Largest SNP chain: 135.0 | mtDNA: T2b | |
Carthago-Maghrebi Andalusia | 1400 AD (I8146) | Genetic Distance: 6.021 | mtDNA: H3a1 | ||
Late Medieval Duomo San Nicola Sardinia | 1450 AD (SNN003) | Genetic Distance: 7.305 | mtDNA: H3f1 | ||
Post Roman Miroico Portugal | 520 AD (R10503) | Genetic Distance: 8.653 | mtDNA: ? | Y-DNA: R1b1a1b1a1a2a | |
Iron Age Polizzello Sicily | 500 BC (I13128) | Genetic Distance: 8.78 | mtDNA: T2b3+151 | Y-DNA: R1b1a1b1a1a2a | |
Phoenician/Punic Sardinia Mount Sirai | 675 BC (MSR003) | Genetic Distance: 9.36 | mtDNA: J1c3 | ||
Urziceni Bodrogkeresztur Neolithic Romania | 3700 BC (I18154) | Genetic Distance: 9.642 | mtDNA: H7b | ||
Etruscan Vetulonium Tuscany Italy | 670 BC (VET002) | Genetic Distance: 9.769 | mtDNA: J1c3s2 | Y-DNA: G2a2b2b1a1a |
R1b 10.4%
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Gallic Cenomani Tribe Italy Verona Seminario Vescovile | 300 BC (3220) | Genetic Distance: 17.85 | mtDNA: X2b6 | Y-DNA: R1b1a1b1a1a2b1 | |
Gallic Cenomani Tribe Dog Co-Burial Italy Verona Seminario Vescovile | 300 BC (3227) | Genetic Distance: 21.12 | mtDNA: U5b3 | Y-DNA: R1b1a1b1a2a1 | |
Deep Dive Carthaginian Sardinia Villamar | 250 BC (VIL011) | Total shared SNPs: 135.0 | Largest SNP chain: 135.0 | mtDNA: K1a3a | Y-DNA: R1b1a1b1a2 |
Post Roman Miroico Portugal | 520 AD (R10503) | Genetic Distance: 8.653 | mtDNA: ? | Y-DNA: R1b1a1b1a1a2a | |
Iron Age Polizzello Sicily | 500 BC (I13128) | Genetic Distance: 8.78 | mtDNA: T2b3+151 | Y-DNA: R1b1a1b1a1a2a | |
Etruscan Tarquinii Italy | 225 BC (TAQ017) | Genetic Distance: 11.26 | mtDNA: T2e20a | Y-DNA: R1b1a1b1a |
I2 5.52%
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Bronze Age Beli Breyag Bulgaria | 2500 BC (Bul6) | Genetic Distance: 12.15 | mtDNA: ? | Y-DNA: I2a2 | |
Early Bronze Age Bulgaria Yunatsite | 2770 BC (YUN037) | Genetic Distance: 12.32 | mtDNA: W1h | Y-DNA: I2a1a2b1a | |
Early Bronze Age Bulgaria | 3100 BC (I2176) | Genetic Distance: 13.26 | mtDNA: U1a1 | Y-DNA: I2a2a1b | |
Chalcolithic Romania Bodrogkeresztur Urziceni | 5180 BC (I7126) | Genetic Distance: 13.96 | mtDNA: H | Y-DNA: I2a1b2 | |
Pre-Etruscan Pian Sultano Italy | 1350 BC (R11104) | Genetic Distance: 14.55 | mtDNA: H1c | Y-DNA: I2a1a1a1a | |
Neolithic Orkney Islands | 3220 BC (I7554) | Genetic Distance: 14.75 | mtDNA: J1c9e | Y-DNA: I2a1a2a1a2a | |
Neolithic Rosheim France | 4600 BC (ROS45) | Genetic Distance: 15.52 | mtDNA: H5u | Y-DNA: I2a1a2 | |
Bronze Age Bulgaria Tell Kran Yasanovo | 2000 BC (I19454) | Genetic Distance: 15.65 | mtDNA: U8b1b | Y-DNA: I2a1a2b | |
Imperial Roman Serbia Svilos Krusevlje | 332 AD (R6701) | Genetic Distance: 16.14 | mtDNA: ? | Y-DNA: I2a1b1a2a1a1 | |
Neolithic Bergheim France | 4100 BC (BERG157-7) | Genetic Distance: 16.48 | mtDNA: U5b1c | Y-DNA: I2a1a2 |
G 5.15%
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Etruscan Vetulonium Tuscany Italy | 670 BC (VET002) | Genetic Distance: 9.769 | mtDNA: J1c3s2 | Y-DNA: G2a2b2b1a1a | |
Iron Age Sicani Tribe Polizzello Sicily | 800 BC (I13382) | Genetic Distance: 10.63 | mtDNA: HV1abc | Y-DNA: G2a2b2a1a1c1a1a2 | |
Iron Age Sicani Tribe Polizzello Sicily | 800 BC (I13389) | Genetic Distance: 12.24 | mtDNA: H4a1 | Y-DNA: G2a2b2a1a1c1a1a2 | |
Trypillian Verteba Cave Ukraine | 3500 BC (I2111) | Genetic Distance: 13.36 | mtDNA: HV | Y-DNA: G2a | |
Copper Age Grottina dei Covoloni del Broion Italy | 3000 BC (BRC013) | Genetic Distance: 14.55 | mtDNA: H5a1 | Y-DNA: G2a2b2b1a1 | |
Etruscan Tarquinii Italy | 306 BC (TAQ023) | Genetic Distance: 14.86 | mtDNA: U5b2a3d | Y-DNA: G2a2b2a1a1c1a1 | |
West Sicily Late Bronze Age | 987 BC (I3876) | Genetic Distance: 14.93 | mtDNA: H1-T16189C | Y-DNA: G2a2b2a1a1c1a1 | |
Chacolithic Ivanovo Bulgaria | 4668 BC (I2431) | Genetic Distance: 15.01 | mtDNA: N1b1 | Y-DNA: G2a2b2a1a1c1a |
J 4.14%
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Deep Dive Late Period Ancient Egypt | 650 BC (JK2911) | Total shared SNPs: 59805.0 | Largest SNP chain: 17392.0 | mtDNA: M1a1 | Y-DNA: J2b1 |
Daunian Salapia Apulian Foggia Italy | 500 BC (SAL001) | Genetic Distance: 12.33 | mtDNA: H1+16189 | Y-DNA: J2b2a | |
Carthaginian/Punic Sardinia Villamar | 250 BC (VIL007) | Genetic Distance: 13.1 | mtDNA: K1a3a | Y-DNA: J1a2a1a2d2b2 |
Clan Weir 2.70%
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Gallic Cenomani Tribe Italy Verona Seminario Vescovile Sample #264 | 300 BC (3220) | Genetic Distance: 17.85 | mtDNA: X2b6 | Y-DNA: R1b1a1b1a1a2b1 | |
Etruscan Tarquinii Italy Sample #22 | 199 BC (TAQ018B) | Genetic Distance: 11.71 | mtDNA: W6a | Y-DNA: R1b1a1b1a1a2b1 |
House of Basarab 0.77%
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Dark Ages Italy South Tyrol Malles Burgusio Santo Stefano Sample #372 | 450 AD (2425) | Genetic Distance: 19.1 | mtDNA: H1e | Y-DNA: E1b1b1a1b1a | |
Late Roman Empire Viminacium Serbia Grobalja Necropolis | 250 AD (I15518) | Total shared SNPs: 214.0 | Largest SNP chain: 112.0 | mtDNA: U2e1a1 | Y-DNA: E1b1b1a1b1a |
This is mtDNA distribution of all the samples which match this kit;
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Abstract
Arguments have long suggested that the advent of early farming in the Near East and Anatolia was linked to a ‘Mother Goddess’ cult. However, evidence for a dominant female role in these societies has been scarce. We studied social organisation, mobility patterns and gendered practices in Neolithic Southwest Asia using 131 paleogenomes from Çatalhöyük East Mound (7100-5950 BCE), a major settlement in Central Anatolia with an uninterrupted occupation and an apparent egalitarian structure. In contrast to widespread genetic evidence for patrilocality in Neolithic Europe, the Çatalhöyük individuals revealed no indication of patrilocal mobility. Analysing genetic kin ties among individuals buried in the same house (co-burials) across 35 Çatalhöyük buildings, we identified close ties concentrated within buildings and among neighbours in Çatalhöyük’s Early period, akin to those in the preceding Pre-Pottery Neolithic in Southwest Asia. This pattern weakened over time: by the late 7th millennium BCE, subadults buried in the same building were rarely closely genetically related, despite sharing similar diets. Still, throughout the site’s occupation, genetic connections within Çatalhöyük buildings were much more frequently connected via the maternal than the paternal line. We also identified differential funerary treatment of female subadults compared to those of males, with a higher frequency of grave goods associated with females. Our results reveal how kinship practices changed while key female roles persisted over one thousand years in a large Neolithic community in western Eurasia.
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