A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2659662

Internal ID9579081
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:147014853..147016159hg38UCSC Ensembl
Outerchr5:147014382..147016779hg38UCSC Ensembl
Innerchr5:146394416..146395722hg19UCSC Ensembl
Outerchr5:146393945..146396342hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6155861, essv5785356, essv6367784, essv5423846, essv6010753, essv6294852, essv6142372, essv5552267, essv6079630, essv5777344, essv5898914, essv5924229, essv5848363, essv5825851, essv5616299, essv6270398, essv6181287, essv5783442, essv6003067, essv6228672, essv5501120, essv5464853, essv6243193, essv6274885, essv6004510, essv5697108, essv5508798, essv5742355, essv6202502, essv6216239, essv6434186, essv5767287, essv5516388, essv6297265, essv5470243, essv5750245, essv5614157, essv5940304, essv5973058, essv6473050, essv5619889, essv5487422, essv5898956, essv6526252, essv5841349, essv6074784, essv5734267, essv6096777, essv6558873, essv5690170, essv5822332, essv6288894, essv6339612, essv5639889, essv6305409, essv6386858, essv5964289, essv6476309, essv5580388, essv6051129, essv5399115, essv5674182, essv6136419, essv6002350, essv5595978, essv5922268, essv5679045, essv5664657, essv6514938, essv5579644, essv6291435, essv6474498, essv6272600
SamplesHG00613, NA19012, HG00607, NA19081, HG00705, HG00437, HG00500, HG00464, NA19072, HG00614, NA18953, HG00475, NA18947, NA19010, HG00683, HG00698, HG00581, HG00651, HG00557, NA18965, HG00699, HG00592, HG00543, NA19062, HG00556, NA19085, NA18967, NA19054, NA19076, HG00583, NA19068, HG00692, HG00689, NA19083, NA19066, NA18959, HG00419, NA19056, HG00584, HG00662, NA19000, NA19080, HG00653, NA19005, HG00560, HG00501, HG00478, NA18942, NA18988, HG00512, HG00534, NA19074, NA18974, NA19078, NA19009, HG00580, NA18971, HG00608, HG00654, NA19064, NA18944, NA19063, HG00422, HG00708, HG00693, HG00566, HG00690, HG00442, HG00473, NA19079, NA19087, NA19065, NA19058
Known GenesPPP2R2B
AnalysisNo reference, merging analysis
CommentsHigh quality site
Pubmed ID23128226
Accession Number(s)esv2659662
Sample Size1151
Observed Gain0
Observed Loss73
Observed Complex0

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