20832
FASTA
Metadata
Reference
Data
| identifier | 20832 |
|---|---|
| alternative_identifiers | - |
| country | Turkey |
| continent | Asia |
| region | Anatolia |
| culture | Çatalhöyük |
| epoch | Neolithic |
| group | NENE |
| comment | Middle Neolithic |
| latitude | 37.66666793823242 |
| longitude | 32.82805633544922 |
| sex | F |
| site | Çatalhöyük |
| site_detail | - |
| mt_hg | H+73 |
| ychr_hg | - |
| year_from | -6450 |
| year_to | -6380 |
| date_detail | 6450-6380 calBCE |
| bp | - |
| c14_lab_code | - |
| c14_sample_tag | - |
| c14_layer_tag | True |
| avg_coverage | 6.300000190734863 |
| sequence_source | reconstructed |
| reference | Chyleński et al. 2019. Ancient Mitochondrial Genomes Reveal the Absence of Maternal Kinship in the Burials of Çatalhöyük People and Their Genetic Affinities. Genes, 10(3), 207. (link) |
| data_link | https://www.ncbi.nlm.nih.gov/popset/1561759632 |
| ychr_snps | - |
| mitopathos | [{'allele': '12705T', 'position': 12705, 'status': 'Reported', 'homoplasmy': '<NA>', 'heteroplasmy': '<NA>', 'locus': ['MT-CO1'], 'diseases': ['Possible protective factor for normal tension glaucoma']}, {'allele': '14668T', 'position': 14668, 'status': 'Reported', 'homoplasmy': '+', 'heteroplasmy': '-', 'locus': ['MT-ND6'], 'diseases': ['Depressive Disorder associated']}, {'allele': '8249A', 'position': 8249, 'status': 'Reported', 'homoplasmy': '+', 'heteroplasmy': '-', 'locus': ['MT-CO2'], 'diseases': ['Mitochondrial myopathy']}] |