A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661080



Internal ID9580499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74369859..74370155hg38UCSC Ensembl
chr7:73784189..73784485hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38297
hg19297
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, essv6500083, essv6140108, essv6520690, essv6450344, essv6004544, essv5878994, essv5502255, essv6126819, essv5806817, essv6562232, essv6464027, essv6106667, essv5987201, essv5609178, essv5615173, essv5524905, essv6385119, essv6220633, essv5907976, essv5653438, essv5668592, essv6288977, essv6207684, essv5728243, essv5587873, essv5818766, essv6513832, essv5890570, essv6512500, essv5591914, essv5570845, essv6581558, essv5535437, essv5682559, essv5451337, essv5412982, essv6007762, essv6456758, essv5650608, essv5668506, essv5474301, essv5886890, essv6068554, essv6577957, essv6068948, essv5871892, essv6470503, essv6399779, essv5677195, essv6237091, essv6390386, essv6492750, essv5964260, essv6392585, essv5878238, essv5826439, essv6588149, essv5610868, essv6511595, essv5696430, essv5988885, essv6562849, essv5476585, essv5480526, essv6542789, essv5582542, essv5860646, essv6535930, essv6323196, essv5610290, essv6551843, essv6238819, essv5663029, essv6001437, essv5441957, essv6064244, essv6001211, essv5655292, essv6498401, essv5659349, essv6293621, essv6002425, essv6123291, essv6417704, essv5616245, essv5412024, essv5716970, essv6559808, essv5703210, essv5765912, essv5587765, 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
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661080
Frequency
Sample Size1151
Observed Gain0
Observed Loss109
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer