A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675240



Internal ID9941345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35296788..35296947hg38UCSC Ensembl
chr15:35588989..35589148hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6310466, essv6402477, essv5468576, essv6051738, essv6036119, essv6199915, essv5715756, essv5455220, essv5916861, essv5419762, essv6281353, essv6309466, essv5788474, essv6495806, essv5946000, essv6525528, essv6455444, essv6212728, essv6550993, essv5564060, essv5880635, essv6499156, essv6242024, essv5549855, essv6460399, essv6051464, essv5961776, essv6404284, essv6442743, essv6112592, essv5601151, essv5579733, essv6415371, essv5396091, essv5490353, essv6455870, essv5637859, essv5545158, essv5789222, essv6442374, essv6490012, essv5407776, essv5721956, essv5604230, essv6424352, essv5539290, essv5614281, essv5657004, essv6515136, essv5735975, essv5410602, essv6327917, essv6382449, essv6177156, essv6115224, essv6028884, essv6475508, essv6218771, essv5743649, essv5698615, essv5594125, essv6129726, essv5973487, essv5655174, essv6099505, essv6187767, essv5768737, essv5715064, essv5486197, essv5928872, essv6316974, essv5467618, essv6458120, essv5650600, essv5851134, essv6417451, essv5544549, essv5560964, essv5757504, essv6478874, essv6255882, essv5805032, essv5728873, essv6112405, essv6120015, essv6414582, essv5961922, essv5614060, essv6230245, essv6476375, essv5917506, essv5644164, essv6211066, essv6563260, essv6230258, essv6067410, essv5678203, essv5575008, essv5526919, essv6322064, essv5593642, essv5930099, essv6180945, essv6464578, essv6311550, essv5777165, essv5865346, essv5838123, essv6200831, essv6267760, essv5405449, essv6302431, essv6297238, essv5629594, essv5744437, essv6539098, essv5397668, essv5443873, essv5669910, essv6220648, essv5665970, essv5691073, essv5930371, essv5893902, essv5880575, essv5562043, essv6027829, essv5962154, essv5736885, essv6507340, essv6297283, essv5720156, essv6191916, essv6124935, essv5488472, essv5714662, essv5618203, essv6496018, essv5535010, essv6341214, essv5544127, essv6306120, essv5762355, essv5679224, essv5868043, essv6363157, essv5629530, essv6372328, essv6315581, essv5875981, essv6454314, essv6354712, essv5398421, essv6560305, essv6405008, essv5475778, essv6512305, essv5761800, essv6023904, essv6346986, essv6297154, essv5600746, essv6372880, essv5948896, essv5460792, essv5414162, essv6080688, essv6409076, essv6572693, essv6588562, essv5999471, essv6437676, essv5516415, essv6108401, essv5416755, essv5486421, essv6195487, essv6040016, essv6243246, essv5806718, essv5962165, essv5472870, essv6581251, essv6163635, essv6073892, essv5557337, essv5623929, essv5771865, essv6354165, essv5702539, essv6243762, essv5754661, essv6485018, essv5760030, essv5763930, essv5731009, essv6418634, essv5572914, essv6143228, essv5656931, essv6439633, essv5627488, essv5762875, essv5869326, essv5977706, essv5468503, essv6057076, essv5564941
SamplesNA19223, NA19060, HG00421, HG00656, NA19474, NA18873, HG00698, NA19213, NA18552, NA18983, HG00595, NA18984, HG00472, NA18505, HG01125, HG00628, NA20322, NA18624, NA19463, NA18511, NA19063, NA18522, NA19065, NA18612, NA18549, HG01191, NA19429, NA19074, NA18622, HG00437, NA18562, HG00581, NA18965, NA18620, HG00593, HG00626, NA19394, NA18502, NA19701, HG01441, HG00650, HG00592, HG01356, NA19397, NA18924, HG00608, NA19909, HG00671, NA18861, NA18592, NA18508, HG00559, HG00524, NA18980, NA18599, NA18999, NA18917, NA19359, NA18545, NA19819, NA19393, NA18504, HG00566, NA19377, NA18530, HG00449, NA18870, NA19920, NA18633, HG00693, NA18988, HG00663, NA19446, NA19374, NA18563, NA19373, NA18944, NA18940, NA18550, NA18519, HG00589, HG00501, NA18489, NA18595, HG00702, HG00689, NA18558, HG01492, HG00634, NA18942, NA18618, HG00610, NA18582, NA19088, NA18571, HG01083, HG01365, NA20287, HG00537, NA20291, NA18949, NA18611, NA19404, NA19720, HG00683, HG01170, HG00262, HG01072, NA19371, HG00534, HG00422, HG01440, NA19725, NA19239, NA18557, HG00530, HG00419, NA19789, NA19921, NA19451, NA18638, HG00464, NA18605, HG00629, NA19437, HG00443, NA18538, HG01187, HG01171, NA19707, NA19070, NA18934, HG00596, NA19403, HG00557, HG00428, NA18933, HG00653, NA18956, HG00657, HG00475, NA19717, NA19455, NA20314, HG00556, HG00584, HG00500, NA18579, NA18572, HG00619, HG00692, NA18548, HG00740, NA18907, NA19114, NA20299, NA19084, HG00690, HG00404, HG01197, HG00684, NA12892, HG01101, HG00525, NA19257, NA18555, NA18963, NA19225, NA18523, HG00463, NA19318, NA19395, NA18858, NA18634, NA18541, NA20296, NA19401, NA19729, HG00611, NA18542, NA18533, NA18535, NA19108, NA18961, NA18952, NA19256, NA18517, NA18628, NA19072, HG01253, NA18941, NA19240, HG00473, NA19439, NA19083, HG01108, HG00662, HG00418, NA19085, NA18610, HG01342, HG00620, NA19818, NA19078, HG00707, HG00614, HG00111, HG00478
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675240
Frequency
Sample Size1151
Observed Gain0
Observed Loss208
Observed Complex0
Frequencyn/a


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