A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2661080

Internal ID9580499
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74369859..74370155hg38UCSC Ensembl
chr7:73784189..73784485hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6045843, essv6310611, essv5693058, essv6154119, essv6065904, essv5853702, essv5988145, essv6140108, essv6500083, essv6450344, essv6520690, essv6004544, essv5878994, essv5502255, essv6126819, essv5806817, essv6562232, essv6464027, essv6106667, essv5987201, essv5609178, essv5615173, essv5524905, essv5653438, essv5907976, essv6220633, essv6385119, essv5668592, essv6288977, essv6207684, essv5728243, essv5587873, essv5818766, essv6513832, essv5890570, essv6512500, essv5591914, essv5570845, essv6581558, essv5535437, essv5682559, essv5451337, essv5412982, essv6007762, essv6456758, essv5650608, essv5668506, essv5474301, essv5886890, essv6068554, essv6068948, essv6577957, essv5871892, essv6470503, essv6399779, essv5677195, essv6237091, essv6390386, essv5964260, essv6492750, essv5878238, essv6392585, essv5826439, essv5610868, essv6588149, essv6511595, essv5696430, essv5988885, essv6562849, essv5476585, essv5480526, essv5582542, essv5860646, essv6542789, essv6323196, essv6535930, essv5610290, essv6551843, essv6238819, essv5663029, essv6001437, essv5441957, essv6064244, essv5655292, essv6001211, essv6498401, essv5659349, essv6293621, essv6002425, essv6123291, essv6417704, essv5616245, essv5412024, essv5716970, essv6559808, essv5703210, essv5587765, essv5765912, essv6385191, essv6162400, essv5912317, essv6456729, essv6511519, essv5463759, essv5729689, essv5926119, essv6457625, essv5879063, essv5458753
SamplesHG00323, HG00734, HG01518, NA18595, NA18530, HG00418, HG01072, HG00328, HG00500, HG01173, HG00171, HG00369, NA20510, HG00186, HG00131, NA19003, NA20299, HG01079, HG00463, HG01197, HG01051, HG01365, HG01492, HG01082, HG01488, HG00428, HG00475, HG01174, HG00683, HG01188, HG00334, HG00651, HG00280, HG01101, HG00366, HG00319, HG00253, HG01551, NA18596, NA20586, HG01133, HG00256, HG00342, NA19077, HG01107, NA19463, HG00556, NA19383, HG00250, NA19076, NA20819, HG01375, HG01378, NA18536, NA18623, HG00231, HG00689, HG01124, HG00258, HG00174, HG00284, HG00343, NA19082, HG00373, HG00159, HG00108, HG00653, HG00732, HG00325, NA19002, HG00265, HG00501, HG00672, HG00282, HG01170, HG00232, HG01069, NA18487, HG01080, NA18613, HG00512, HG01149, HG00151, HG01334, HG00138, HG00663, HG00580, HG01112, HG00654, HG01390, HG00281, HG00656, HG00142, HG01366, NA19732, HG00422, HG00708, NA18610, HG00693, NA19756, NA18549, HG00137, HG00336, HG00671, NA19087, HG00271, HG00126, HG01067, HG00361
Known GenesCLIP2
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)esv2661080
Sample Size1151
Observed Gain0
Observed Loss109
Observed Complex0

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