A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660785



Internal ID9926890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:27934279..27936285hg38UCSC Ensembl
Outerchr13:27933908..27936755hg38UCSC Ensembl
Innerchr13:28508416..28510422hg19UCSC Ensembl
Outerchr13:28508045..28510892hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg382848
hg192848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5663832, essv6357451, essv6232932, essv6451102, essv6483472, essv6068301, essv6522076, essv5990620, essv5978779, essv6422592, essv6186471, essv5823497, essv6221696, essv6494557, essv5910697, essv5526755, essv6105721, essv6293090, essv5879595, essv5590024, essv6235036, essv5552486, essv6061827, essv6204328, essv6328115, essv6577463, essv5435685, essv6221918, essv6447098, essv5621690, essv6277311, essv6586566, essv6047289, essv6368585, essv5946341, essv5544206, essv6424921, essv5409186, essv6531955, essv6299601, essv5995960, essv5863388, essv5972728, essv5638716, essv5456215, essv5922852, essv6064218, essv5727375, essv6578427, essv5764159, essv5825602, essv6353429, essv6004881, essv5593808, essv5925631, essv5604021, essv5862614, essv6367331, essv5701777, essv5423245, essv5752663, essv6441715, essv6294599, essv6286544, essv5613598, essv5633294, essv6371125, essv5558186, essv6206060, essv6183392, essv6546310, essv5399743, essv6244332, essv6215324, essv6131696, essv6468188, essv5643914, essv6130255, essv5957980, essv5924867, essv5920935, essv5517809, essv5885203, essv6270348, essv6083788, essv5704549, essv6133675, essv5676963, essv6212805, essv5433446, essv6119211, essv6004950, essv5981563, essv6482052, essv6241428, essv5922797, essv5439111, essv6494853, essv5960113, essv5415627, essv5835640, essv6540878, essv6527112, essv6149969, essv5478779, essv5585572, essv5645195, essv6286659, essv6411663, essv5583645, essv6348731, essv5829075, essv6145723, essv5859724, essv6567543, essv5497887, essv5744392, essv6160390, essv5854902, essv6208527, essv6159521, essv6584486, essv6520137, essv5620029, essv6429213, essv6248519, essv6105182, essv6521401, essv5773280, essv5458455, essv5489539, essv5431508
SamplesHG00593, HG00626, HG00403, HG01060, HG00650, HG00542, HG00442, HG01173, HG00536, HG00608, HG00671, HG00524, HG01052, HG01079, HG01188, HG01066, HG00640, HG00699, HG00566, HG00737, HG00449, HG00654, HG01051, HG00693, HG00663, HG00641, HG01070, HG00589, HG00501, HG01167, HG00702, HG00689, HG00448, HG00736, HG00610, HG01083, HG00537, HG00590, HG00512, HG01069, HG01080, HG01067, HG00683, HG01170, HG01072, HG00534, HG00422, HG01176, HG00705, HG00427, HG01198, HG01048, HG00530, HG00419, HG00464, HG00543, HG01183, HG00560, HG00731, HG00443, HG01187, HG01171, HG00596, HG00557, HG00428, HG00732, HG00653, HG00577, HG01095, HG00701, HG00657, HG00475, HG00436, HG00556, HG00584, HG00533, HG00583, HG00500, HG00619, HG00708, HG00692, HG00740, HG01047, HG01102, HG01073, HG00651, HG00690, HG00404, HG00531, HG00479, HG01197, HG00684, HG01182, HG01101, HG00613, HG00525, HG00704, HG00463, HG01107, HG01204, HG01075, HG00476, HG01190, HG00565, HG00580, HG00734, HG00638, HG01174, HG00473, HG00607, HG01108, HG00662, HG00418, HG00620, HG00707, HG00672, HG00614, HG00513, HG00578, HG00478, HG00421, HG00656, HG01055, HG00698, HG00472, HG01082, HG00628, HG01191, HG01061, HG00553, HG00437, HG00581
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660785
Frequency
Sample Size1151
Observed Gain0
Observed Loss132
Observed Complex0
Frequencyn/a


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