A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2668480

Internal ID9587899
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11854051..11855011hg38UCSC Ensembl
chr11:11875598..11876558hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6035102, essv6342292, essv5932255, essv6556936, essv6074314, essv6534123, essv6225136, essv5813404, essv6428009, essv5981769, essv6172643, essv5923516, essv5863470, essv6187055, essv5783568, essv5946327, essv5651920, essv5679091, essv6328502, essv6095293, essv5682247, essv6027740, essv6537150, essv6395913, essv5434771, essv5770388, essv5406769, essv5756833, essv6040324, essv6231691, essv5901381, essv5428976, essv5578034, essv6054110, essv6073878, essv6111038, essv6417181, essv6519582, essv5617976, essv6046456, essv5733820, essv6551963, essv6285466, essv5637058, essv6412774, essv6521085, essv6597009, essv5444572, essv5515601, essv5701890, essv5898182, essv6055776, essv6117230, essv5812484, essv6248986, essv5747367, essv5834092, essv6188167, essv5647053, essv6467647, essv6570999, essv5471701, essv5437551, essv5900194, essv5970440, essv5927867, essv6393849, essv5404228, essv6167494, essv6458056, essv5552837, essv5978466, essv5430297, essv5632931, essv5486162, essv6387000, essv6454812, essv5539785, essv5465958, essv6079036, essv6446085, essv6219741, essv6504145, essv5884690, essv5660988, essv5459581, essv6343586, essv6401089, essv6234652, essv5768858, essv5919796, essv5645989, essv6215414, essv5511135, essv5765596, essv6133840, essv6390567, essv6191268, essv5496887, essv6405545, essv6596336, essv5999456, essv5933174, essv6486605, essv6296218, essv5858692, essv5569038, essv5415004, essv6014055, essv5422693, essv5823138, essv6077528, essv5947944, essv6301220, essv6520039, essv6167195, essv5450764, essv6444912, essv5799952, essv6008064, essv6516836, essv6164130, essv5936834, essv5927677, essv6444678, essv5779356, essv5659665, essv6072495, essv6562276, essv6187896, essv6446122, essv6318322, essv6215823, essv5985141, essv6114936, essv6348195, essv6581754, essv6274215, essv5679767, essv5621059, essv6395151, essv5909624, essv6433232, essv6009349, essv6512764, essv5551439, essv6051907, essv6559886, essv6082388, essv5762122
SamplesNA20281, NA18621, HG00309, NA18964, HG00313, NA19625, HG01359, HG00252, NA18535, HG00418, NA12286, NA19081, HG00437, HG00171, HG00131, NA19060, HG01098, NA20296, HG00189, NA20808, HG01488, HG00375, HG01174, NA20778, HG00270, NA18541, HG00122, NA18546, HG00106, NA20805, HG00581, NA18963, NA19685, HG00404, NA19651, HG00651, NA19004, HG00557, HG01101, HG01134, HG00578, HG00177, HG00331, HG00253, HG00699, NA20755, HG00353, HG00342, HG00592, HG00635, NA18559, HG00339, NA19085, NA19059, NA19076, NA20819, HG00472, HG00583, NA19660, HG00259, NA18563, NA20757, HG01048, HG00610, NA18990, HG00692, HG01183, HG01047, NA18636, HG01124, NA18592, NA19088, HG00330, NA19398, HG00149, HG00178, HG00258, HG01113, NA19773, HG00357, NA18634, NA19082, NA20341, HG00662, NA20769, HG00436, HG00159, HG00620, NA19080, NA07346, HG01465, NA19759, HG00640, NA20126, HG00732, NA20753, HG01455, NA12275, NA19005, HG01073, HG00273, HG01170, HG00277, HG00513, NA20542, NA19707, NA19074, NA18579, NA20813, HG00589, NA18543, HG01137, HG00595, NA20534, NA19078, HG01334, HG00138, HG00663, HG00262, HG00608, HG01390, NA19452, NA20513, NA19063, NA12399, HG00656, NA12546, NA18610, NA18984, HG00566, NA19346, NA20768, HG00119, HG00324, HG00641, NA18574, HG00137, HG01489, HG00626, HG00143, HG00336, HG00671, NA19087, HG00272, NA20538, NA18555, HG00271, NA19007, HG00312, HG01198
Known GenesUSP47
AnalysisNo reference, merging analysis
CommentsHigh quality site
Pubmed ID23128226
Accession Number(s)esv2668480
Sample Size1151
Observed Gain0
Observed Loss150
Observed Complex0

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