A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677760



Internal ID9943865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27099337..27101343hg38UCSC Ensembl
Outerchr6:27098966..27101713hg38UCSC Ensembl
Innerchr6:27067116..27069122hg19UCSC Ensembl
Outerchr6:27066745..27069492hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg382748
hg192748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5855668, essv5957395, essv5687534, essv5710997, essv5710423, essv5765841, essv6408131, essv6385887, essv5995947, essv6390683, essv5696197, essv6070686, essv5559638, essv5443415, essv5843055, essv5638439, essv5526177, essv5415628, essv5560668, essv6054871, essv5496707, essv6474473, essv6094064, essv5793058, essv5629548, essv5877197, essv6421192, essv6151756, essv5496770, essv6319562, essv6202671, essv5965433, essv5827344, essv6320224, essv5509080, essv6366379, essv5953530, essv6407744, essv5749151, essv6071338, essv5523851, essv6238172, essv6222338, essv5863220, essv5441856, essv5808417, essv6235631, essv6166206, essv6240266, essv6221817, essv6435850, essv6462129, essv6099247, essv5712080, essv6469240, essv5767053, essv6443138, essv5983826, essv5644574, essv6488464, essv5956786, essv5706559, essv6416123, essv6033963, essv5513779, essv5464849, essv6199908, essv5964693, essv5658570, essv5924717, essv6343899, essv6228181, essv5467534, essv5931511, essv5848141, essv5500946, essv6572810, essv6112994, essv5538772, essv6253854, essv6328987, essv6417344, essv6382257, essv6293771, essv6554772, essv5596282, essv5751573
SamplesHG00593, HG00626, HG00403, HG00650, HG00542, HG00442, HG00536, HG00608, HG00671, HG00559, HG00524, HG00699, HG00566, HG00449, HG00654, HG00693, HG00663, HG00589, HG00501, HG00702, HG00448, HG00634, HG00610, HG00537, HG00590, HG00512, HG00683, HG00534, HG00422, HG00705, HG00427, HG00530, HG00419, HG00464, HG00543, HG00629, HG00443, HG00596, HG00557, HG00428, HG00653, HG00577, HG00701, HG00657, HG00475, HG00436, HG00556, HG00584, HG00533, HG00583, HG00500, HG00619, HG00708, HG00692, HG00635, HG00651, HG00690, HG00404, HG00531, HG00479, HG00684, HG00613, HG00525, HG00704, HG00463, HG00611, HG00476, HG00565, HG00580, HG00473, HG00607, HG00662, HG00418, HG00620, HG00707, HG00672, HG00614, HG00513, HG00578, HG00478, HG00421, HG00656, HG00698, HG00472, HG00628, HG00437, HG00581
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677760
Frequency
Sample Size1151
Observed Gain0
Observed Loss87
Observed Complex0
Frequencyn/a


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