A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668480



Internal ID9587899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11854051..11855011hg38UCSC Ensembl
chr11:11875598..11876558hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38961
hg19961
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, essv6428009, essv5813404, essv5981769, essv6172643, essv5923516, essv5863470, essv6187055, essv5946327, essv5783568, essv5651920, essv5679091, essv6328502, essv6095293, essv5682247, essv6027740, essv6537150, essv6395913, essv5434771, essv5770388, essv5406769, essv6040324, essv6231691, essv5756833, essv5428976, essv5578034, essv5901381, essv6054110, essv6073878, essv6111038, essv6417181, essv6519582, essv5617976, essv6046456, essv5733820, essv6551963, essv6285466, essv5637058, essv6412774, essv6597009, essv6521085, essv5444572, essv5515601, essv5701890, essv5898182, essv6117230, essv6055776, essv5812484, essv6248986, essv5747367, essv5834092, essv6188167, essv5647053, essv6467647, essv6570999, essv5471701, essv5970440, essv5437551, essv5900194, essv5927867, essv6393849, essv5404228, essv6167494, essv6458056, essv5552837, essv5978466, essv5430297, essv5632931, essv5486162, essv6387000, essv6454812, essv5539785, essv6079036, essv5465958, essv6446085, essv6219741, essv6504145, essv5884690, essv5660988, essv5459581, essv6343586, essv6401089, essv6234652, essv5768858, essv5919796, essv6215414, essv5645989, essv6133840, essv5511135, essv5765596, essv6390567, essv6191268, essv5496887, essv6596336, essv6405545, essv5999456, essv5933174, essv6486605, essv6296218, essv5858692, essv5569038, essv5415004, essv6014055, essv6077528, essv5823138, essv5422693, essv5947944, essv6301220, essv6520039, essv6167195, essv6444912, essv5450764, essv5799952, essv6008064, essv6516836, essv6164130, essv5927677, essv5936834, essv6444678, essv5779356, essv5659665, essv6072495, essv6562276, essv6446122, essv6187896, essv6318322, essv6215823, essv5985141, essv6114936, essv6581754, essv6348195, 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
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668480
Frequency
Sample Size1151
Observed Gain0
Observed Loss150
Observed Complex0
Frequencyn/a


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