A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671903



Internal ID9591322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65538645..65540451hg38UCSC Ensembl
Outerchr11:65538274..65540821hg38UCSC Ensembl
Innerchr11:65306116..65307922hg19UCSC Ensembl
Outerchr11:65305745..65308292hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382548
hg192548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6204583, essv6427532, essv5879665, essv6412709, essv5940061, essv6091667, essv5616994, essv6441238, essv6506902, essv5505933, essv6270524, essv6282350, essv6443803, essv6080565, essv6446669, essv6572435, essv5679876, essv6596314, essv6122515, essv6362981, essv6283047, essv5853103, essv5442376, essv6297914, essv6406200, essv6349765, essv6586856, essv5663336, essv6567550, essv6177935, essv6529006, essv6017707, essv6151547, essv5692962, essv6494638, essv5644555, essv5459864, essv5954635, essv6162820, essv5587671, essv6381744, essv6527249, essv6010572, essv6294274, essv5498292, essv6012595, essv5552088, essv5797003, essv6408735, essv6237074, essv5808931, essv6543357, essv6555600, essv5672541, essv6541792, essv5723668, essv6351718, essv6244437, essv6278740, essv6241029, essv5980188, essv5865221, essv6466033, essv5992822, essv6271869, essv5438012, essv6413568, essv6373235, essv6076445, essv5816221, essv6458091, essv6340761, essv5689626, essv6508178, essv5563084, essv5692210, essv5747464, essv5785466, essv6290588, essv5839363, essv5687136, essv5581403, essv6533059, essv6150055, essv5464557, essv6213827, essv6386561, essv6050320, essv5875021, essv5819219, essv5475033, essv6322111, essv5896421, essv6047426, essv6143411, essv6303983, essv5812485, essv6364495, essv5653238, essv6389161, essv6503731, essv5440958, essv5763887, essv5746541, essv5779750, essv5628787, essv5399299, essv5401689, essv5686127, essv6429493, essv5917971, essv6113033, essv5895234, essv6329987, essv6077348, essv6132388, essv5787901, essv6016156, essv5750002, essv6009105, essv5847576, essv5940326, essv6290566, essv5509384, essv6021050, essv6477017, essv5588779, essv5892343, essv5892821, essv5425317, essv6589590, essv5412943, essv5636164, essv6003445, essv6204308, essv5793109, essv6133126, essv6280767, essv6388072
SamplesHG00626, HG00403, HG00650, HG00542, HG00442, HG00536, HG00608, HG00671, HG00361, HG00524, HG00315, HG00318, HG00181, HG00699, HG00449, HG00654, HG00337, HG00327, HG00271, HG00663, HG00589, HG00272, HG00501, HG00702, HG00689, HG00448, HG00330, HG00610, HG00346, HG00334, HG00537, HG00590, HG00512, HG00281, HG00277, HG00683, HG00335, HG00325, HG00534, HG00422, HG00705, HG00309, HG00182, HG00427, HG00338, HG00326, HG00178, HG00323, HG00530, HG00419, HG00464, HG00543, HG00313, HG00629, HG00443, HG00268, HG00266, HG00183, HG00176, HG00282, HG00596, HG00557, HG00328, HG00428, HG00653, HG00701, HG00657, HG00475, HG00368, HG00436, HG00556, HG00320, HG00584, HG00533, HG00583, HG00344, HG00500, HG00275, HG00619, HG00708, HG00692, HG00635, HG00324, HG00284, HG00273, HG00651, HG00690, HG00404, HG00373, HG00531, HG00479, HG00331, HG00684, HG00613, HG00525, HG00321, HG00276, HG00704, HG00463, HG00611, HG00476, HG00336, HG00285, HG00625, HG00565, HG00353, HG00580, HG00375, HG00278, HG00473, HG00607, HG00319, HG00662, HG00418, HG00620, HG00339, HG00269, HG00707, HG00672, HG00614, HG00513, HG00478, HG00421, HG00329, HG00656, HG00342, HG00267, HG00310, HG00186, HG00698, HG00280, HG00343, HG00274, HG00595, HG00472, HG00345, HG00180, HG00437, HG00581
Known GenesLTBP3, SCYL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671903
Frequency
Sample Size1151
Observed Gain0
Observed Loss139
Observed Complex0
Frequencyn/a


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