A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660426



Internal ID9926531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33753234..33753795hg38UCSC Ensembl
Outerchr6:33753195..33753852hg38UCSC Ensembl
Innerchr6:33721011..33721572hg19UCSC Ensembl
Outerchr6:33720972..33721629hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5916196, essv6041392, essv6371829, essv5456974, essv5963883, essv5549796, essv6077922, essv5502251, essv5875200, essv5801641, essv6109371, essv5963458, essv5436512, essv5887796, essv5434809, essv5579253, essv5741605, essv5729937, essv5672517, essv6220982, essv5607741, essv6379178, essv5778995, essv6265816, essv5947815, essv5792765, essv6500758, essv6589077, essv5813913, essv6404485, essv5518368, essv6118306, essv6233445, essv5869000, essv5503170, essv5791917, essv6345267, essv5822855, essv6476019, essv5424696, essv5561150, essv6070668, essv6223054, essv6026168, essv5792602, essv6243708, essv6256196, essv5955054, essv6044499, essv5901078, essv6417521, essv6550344, essv6433710, essv6142416, essv6361222, essv5540140, essv6470206, essv6590760, essv6394369, essv6205852, essv6525722, essv6380995, essv5801410, essv5996119, essv6202378, essv5505879, essv6303256, essv5484578, essv6132058, essv5776659, essv5488889, essv6005450, essv5756436, essv6282167, essv6039970, essv6291195, essv6188439, essv5820435, essv5403303, essv5562837, essv5436987, essv6577008, essv6526984, essv6494038, essv6254682, essv5569424, essv6348125, essv6221334, essv5430278, essv6516000, essv6505408, essv5700931, essv5955232, essv6018855, essv6229810, essv6381240, essv6511087, essv6570335, essv6415819, essv5997994, essv5902837, essv5648812, essv5557696, essv6311811, essv5450209, essv6456828, essv6367930, essv5857639, essv6409416, essv5621253, essv5836135, essv6068757, essv6091963, essv5745951, essv5722433, essv5761078, essv5569302, essv6444770, essv6492237, essv6177311, essv5515153, essv6242041, essv5857443, essv5816825, essv6416875, essv5672402, essv5667889, essv6427192, essv6036583, essv6504491, essv5926185, essv5568442, essv5421338, essv6036841, essv6151019, essv6135892, essv6255647, essv6587003, essv6274595, essv5864384, essv5443558, essv6177680, essv6375080, essv5650652, essv5954213, essv6444931, essv6111474, essv6492297, essv6131643, essv5846544, essv5591424, essv6457465, essv5517633, essv6147034, essv5719932, essv6106265, essv5999353, essv5748519, essv6513228, essv6358388, essv6533235, essv6224564, essv5903739, essv6136386, essv6554072, essv6159034, essv6218353, essv6447978, essv6369208, essv6340315, essv6320981, essv5782989, essv5510740, essv5810706, essv5638178, essv6388284, essv5664023, essv5591855, essv5532770, essv5776278, essv5926361, essv5656376, essv5597426, essv6489602, essv5799367, essv6457906, essv6567245, essv6058576, essv5769701, essv5795077, essv6452455, essv5874390, essv5815805, essv6165048, essv6055618, essv5688342, essv6543039, essv5944105, essv5622474, essv5538151, essv5425310, essv5841259, essv6197816, essv6217064, essv5442044, essv6074311, essv5998540
SamplesHG00403, NA12383, HG00114, NA19701, NA20761, HG00542, NA19648, NA19058, HG01521, NA12842, NA20766, NA18947, NA12286, HG00249, HG00361, HG00524, NA20783, NA18565, HG01079, NA20514, NA11933, NA18599, HG00315, NA18999, HG00640, NA18486, HG00699, NA19355, NA18625, NA12058, NA18959, NA12400, NA19920, NA20771, NA12750, NA18602, NA18988, NA12413, NA19107, NA20814, NA20537, NA07346, HG01250, NA19373, NA19076, NA20796, NA19379, NA19005, NA18944, NA18550, HG00272, NA19315, NA18597, NA18489, NA19678, NA18567, HG00634, NA19062, NA07048, NA11918, NA07347, HG00346, NA19088, HG01083, NA18498, NA19782, NA19904, NA18964, HG00311, NA20291, NA19130, NA19079, NA20759, HG00277, NA20775, NA06984, HG00236, NA20812, NA18868, NA18560, NA19385, HG00422, NA19471, HG00705, NA18986, NA19722, NA19002, HG00427, NA20811, NA18520, HG00637, NA18557, NA18985, NA20533, HG00323, HG00530, HG00419, NA19789, HG00464, HG00260, NA19007, HG00543, HG00313, HG00133, HG01136, NA20535, NA19247, NA19657, NA18538, HG00268, NA19082, HG01171, HG00380, HG00282, NA19070, HG01384, NA19403, HG00245, NA12342, NA12003, NA20521, NA20760, NA19982, HG00320, HG00533, NA19064, HG00740, HG01047, HG00273, NA19774, NA19655, HG00531, NA20581, NA11893, NA18856, NA12249, NA19750, NA06989, HG01497, NA20282, NA18555, NA18963, NA20828, NA19469, NA12778, NA19675, NA18541, NA20765, NA20296, HG01148, NA19003, HG00258, NA20799, NA18542, HG00155, NA20801, NA18533, NA12716, NA18535, NA19834, NA18952, NA19749, NA20815, NA18950, HG00375, HG00357, HG00136, NA20804, NA19773, NA19380, NA07051, NA20785, NA19010, HG01174, NA20778, NA19786, NA20516, NA19083, NA20803, NA19085, NA18615, NA06986, HG00339, NA19759, NA19376, NA19398, HG00513, NA20348, NA20582, NA19472, NA19779, HG00421, NA12830, NA19770, NA11843, NA20826, NA19780, NA19900, HG01251, NA19004, NA18488, NA12890, NA19065, HG01112, NA19074, HG00437, NA18577
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660426
Frequency
Sample Size1151
Observed Gain0
Observed Loss207
Observed Complex0
Frequencyn/a


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