A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2676776

Internal ID9596195
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:37097615..37102321hg38UCSC Ensembl
Outerchr15:37097244..37102791hg38UCSC Ensembl
Innerchr15:37389816..37394522hg19UCSC Ensembl
Outerchr15:37389445..37394992hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5442347, essv5446965, essv5828913, essv6176320, essv5458108, essv5835675, essv6309494, essv6208466, essv5953347, essv6596130, essv5794034, essv6191715, essv6498097, essv5870732, essv6437826, essv5412784, essv6395451, essv6223989, essv5749637, essv6218975, essv6216506, essv5454505, essv6583627, essv5716499, essv6136659, essv6338448, essv6147361, essv6041802, essv5894299, essv5873703, essv5979462, essv6497609, essv5724468, essv5412511, essv6591465, essv5855150, essv5866448, essv6340837, essv6553381, essv5743955, essv5842891, essv6568493, essv6338686, essv5963112, essv6560919, essv5532977, essv5492081, essv5626651, essv6142724, essv5458785, essv5438960, essv5819497, essv5924868, essv6469660, essv6469101, essv6015124, essv5739661, essv6523520, essv5588877, essv5950241, essv5888495, essv5577283, essv5471118, essv6129444, essv6480417, essv6315603, essv5928261, essv5681175, essv5947858, essv6203693, essv5583703, essv6448497, essv5554216, essv5648864, essv5902137, essv6135262, essv6099112, essv6033925, essv5791171, essv5640631, essv6488781, essv6064132, essv6128484, essv6362902, essv5643725, essv5964628, essv6221931, essv5825998, essv6408914, essv5931936, essv6163448, essv6208777, essv5471619, essv5593033, essv5446424, essv5511620, essv6051537, essv5831828, essv5939381, essv6172890, essv6396010, essv6181281, essv6430736, essv5506714, essv5955205, essv5916392, essv6233206, essv5573835, essv6472202, essv6224769, essv6240343, essv5868373, essv5884119, essv6573937, essv5767742, essv6178196, essv6036713, essv5873988, essv5456339, essv6204986, essv5824130, essv5678882, essv6596743, essv5459055, essv6390435, essv6372789, essv5980134, essv6085888, essv6372611, essv6242228, essv5600351, essv5583437, essv6222653, essv6458079, essv5453597, essv6383884, essv5529051, essv5719707
SamplesHG00323, HG00613, HG00309, HG00313, HG00537, HG00318, HG00536, HG00607, HG00182, HG00344, HG00418, HG00328, HG00705, HG00500, HG00171, HG00369, HG00274, HG00186, HG00464, HG00596, HG00449, HG00310, HG00707, HG00463, HG00657, HG00614, HG00189, HG00428, HG00475, HG00542, HG00368, HG00173, HG00326, HG00270, HG00190, HG00701, HG00683, HG00581, HG00187, HG00404, HG00651, HG00280, HG00335, HG00557, HG00366, HG00578, HG00177, HG00331, HG00319, HG00699, HG00188, HG00353, HG00479, HG00269, HG00592, HG00266, HG00543, HG00339, HG00556, HG00346, HG00179, HG00472, HG00421, HG00583, HG00337, HG00180, HG00610, HG00692, HG00628, HG00338, HG00533, HG00178, HG00419, HG00634, HG00284, HG00403, HG00357, HG00343, HG00584, HG00373, HG00436, HG00267, HG00620, HG00653, HG00268, HG00629, HG00185, HG00559, HG00176, HG00501, HG00273, HG00282, HG00478, HG00513, HG00524, HG00329, HG00512, HG00525, HG00377, HG00589, HG00427, HG00590, HG00595, HG00443, HG00181, HG00650, HG00663, HG00448, HG00654, HG00530, HG00281, HG00285, HG00656, HG00422, HG00708, HG00367, HG00693, HG00566, HG00320, HG00275, HG00625, HG00690, HG00442, HG00473, HG00626, HG00684, HG00336, HG00476, HG00671, HG00272, HG00345, HG00704, HG00271, HG00278, HG00531, HG00312, HG00327, HG00361
Known GenesMEIS2
AnalysisNo reference, merging analysis
CommentsHigh quality site
Pubmed ID23128226
Accession Number(s)esv2676776
Sample Size1151
Observed Gain0
Observed Loss138
Observed Complex0

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