A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676776



Internal ID9942881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:37097615..37102321hg38UCSC Ensembl
Outerchr15:37097244..37102791hg38UCSC Ensembl
Innerchr15:37389816..37394522hg19UCSC Ensembl
Outerchr15:37389445..37394992hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg385548
hg195548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5511620, essv6085888, essv6222653, essv6591465, essv5743955, essv5828913, essv5739661, essv6233206, essv5454505, essv5855150, essv5573835, essv6372611, essv5831828, essv6472202, essv6553381, essv6596743, essv5963112, essv6135262, essv5492081, essv5955205, essv6437826, essv6142724, essv5928261, essv5643725, essv6216506, essv5953347, essv6315603, essv5458785, essv6497609, essv6242228, essv5724468, essv6469660, essv5979462, essv6136659, essv5719707, essv5588877, essv6128484, essv6172890, essv5866448, essv6372789, essv5980134, essv5456339, essv5446424, essv6129444, essv6204986, essv6573937, essv6208777, essv6395451, essv6223989, essv6099112, essv6448497, essv6340837, essv6033925, essv5412511, essv5916392, essv5471118, essv5873988, essv6383884, essv6064132, essv6203693, essv5532977, essv6178196, essv5577283, essv5600351, essv5749637, essv5459055, essv5453597, essv5593033, essv5964628, essv6568493, essv6408914, essv6480417, essv6458079, essv5947858, essv5458108, essv5842891, essv5678882, essv5931936, essv6583627, essv5870732, essv5640631, essv5442347, essv5471619, essv6036713, essv5825998, essv6390435, essv5902137, essv5819497, essv6596130, essv6181281, essv5884119, essv5648864, essv5894299, essv5716499, essv6396010, essv5924868, essv6191715, essv5767742, essv6240343, essv5681175, essv6338686, essv6221931, essv5446965, essv6523520, essv6218975, essv5438960, essv6041802, essv6208466, essv6338448, essv5939381, essv5888495, essv6176320, essv6498097, essv6309494, essv5554216, essv6362902, essv6051537, essv6015124, essv5835675, essv5950241, essv5583437, essv5626651, essv6488781, essv6560919, essv5873703, essv6469101, essv6224769, essv6163448, essv5529051, essv5506714, essv5868373, essv6147361, essv5791171, essv5794034, essv5412784, essv5824130, essv6430736, essv5583703
SamplesHG00626, HG00403, HG00189, HG00650, HG00542, HG00442, HG00592, HG00536, HG00671, HG00361, HG00559, HG00524, HG00187, HG00367, HG00318, HG00181, HG00699, HG00566, HG00179, HG00449, HG00177, HG00654, HG00693, HG00337, HG00327, HG00271, HG00663, HG00589, HG00272, HG00501, HG00448, HG00173, HG00634, HG00610, HG00346, HG00369, HG00270, HG00185, HG00537, HG00590, HG00512, HG00281, HG00683, HG00335, HG00422, HG00705, HG00309, HG00182, HG00427, HG00338, HG00326, HG00178, HG00323, HG00530, HG00419, HG00464, HG00543, HG00313, HG00188, HG00629, HG00443, HG00268, HG00266, HG00176, HG00282, HG00596, HG00557, HG00328, HG00428, HG00190, HG00653, HG00701, HG00657, HG00475, HG00368, HG00436, HG00556, HG00320, HG00584, HG00533, HG00583, HG00344, HG00500, HG00275, HG00708, HG00692, HG00284, HG00273, HG00651, HG00690, HG00404, HG00373, HG00531, HG00479, HG00331, HG00684, HG00613, HG00525, HG00704, HG00463, HG00476, HG00336, HG00285, HG00625, HG00366, HG00353, HG00357, HG00278, HG00473, HG00607, HG00319, HG00418, HG00620, HG00339, HG00269, HG00707, HG00614, HG00513, HG00578, HG00478, HG00312, HG00421, HG00329, HG00656, HG00267, HG00310, HG00186, HG00280, HG00343, HG00377, HG00274, HG00595, HG00472, HG00628, HG00171, HG00345, HG00180, HG00581
Known GenesMEIS2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676776
Frequency
Sample Size1151
Observed Gain0
Observed Loss138
Observed Complex0
Frequencyn/a


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