A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672815



Internal ID9938920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:17376618..17381023hg38UCSC Ensembl
Outerchr6:17376461..17381176hg38UCSC Ensembl
Innerchr6:17376849..17381254hg19UCSC Ensembl
Outerchr6:17376692..17381407hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384716
hg194716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1076e199
Supporting Variantsessv5396970, essv6517637, essv6221323, essv6205344, essv6351241, essv6185805, essv5825401, essv6168470, essv6244063, essv5414285, essv5548056, essv5965253, essv6263906, essv5747886, essv5671987, essv6415200, essv6298009, essv5596131, essv5825699, essv5686418, essv5755885, essv5447018, essv6578932, essv5442310, essv5860324, essv6587972, essv5989497, essv6127720, essv5859386, essv6273733, essv5973833, essv5812366, essv5972949, essv6510697, essv5403866, essv5726665, essv5741169, essv5879602, essv5531809, essv6012586, essv5903376, essv5716260, essv5673092, essv5660258, essv6215193, essv6157155, essv5647857, essv5926395, essv6312918, essv6094806, essv5816815, essv5511441, essv5845715, essv6285918, essv6287781, essv5616597, essv5929653, essv5917691, essv6290421, essv6065414, essv6236665, essv6027206, essv6317937, essv5922484, essv5593671, essv5743379, essv6358430, essv6090698, essv6399646, essv6244079, essv5796299, essv5755821, essv6130785, essv6108328, essv5808577, essv5609236, essv6371089, essv6505918, essv5979499, essv5422705, essv6033373, essv5800016, essv6372527, essv5756282, essv5432607, essv5976427, essv6002159, essv5850969, essv6130492, essv5762414, essv5792805, essv6012162, essv5765314, essv5848871, essv6428967, essv5873493, essv5579222, essv5426278, essv5942380, essv6391303, essv6058627, essv6533431, essv6548709, essv6053993, essv5736123, essv6006697, essv5898873, essv5736117, essv5493790, essv6039612, essv6038766, essv6477731, essv5579285, essv6594615, essv5748876, essv5804146, essv5638340, essv5576673, essv5496506, essv5407220, essv5628442, essv6569427, essv5537198, essv6079322, essv5710388, essv6044050, essv5971665, essv5758626, essv5852993, essv6377025, essv5878459, essv5494431
SamplesNA19394, HG00542, NA19648, HG00143, NA19703, NA19332, HG00100, HG01188, HG00151, NA20813, HG01465, NA19819, NA20808, HG00177, HG00654, HG01051, HG01140, HG00327, NA20814, HG00138, NA19373, NA19076, HG01070, HG00251, HG00122, NA18597, HG00173, NA19723, HG00736, NA07048, HG00346, NA19313, HG00247, NA19054, HG00243, NA19079, HG00590, HG00139, NA12275, HG00120, NA19383, HG00106, HG01170, NA20812, HG00232, NA19731, HG00705, HG01440, HG00309, HG00118, HG01133, HG00326, HG00178, NA20127, HG00323, HG00253, NA19921, HG01124, HG00313, HG00137, HG01136, HG00188, NA18605, HG00731, HG00176, NA19707, NA19403, HG00557, NA12342, HG00732, HG00275, NA12718, NA18572, HG01149, NA19776, HG00708, HG00692, NA19064, HG01390, HG00324, NA11919, NA20299, NA20581, HG00331, HG00684, HG01383, HG01101, NA19059, NA19761, HG00152, NA18523, HG00463, NA12778, HG00126, HG01075, HG00124, NA19652, HG00265, HG00565, HG00366, NA20815, HG00357, HG00278, NA07051, HG01375, NA19786, HG00319, HG00116, NA19083, HG01108, NA07037, NA19376, NA19716, NA19474, HG01055, HG00280, NA19116, HG01251, NA20503, HG01377, NA19312, HG00171, NA20322, NA18623, NA20585, NA19065, HG01191, NA18487, HG01437, HG01061, HG00553, HG00581
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672815
Frequency
Sample Size1151
Observed Gain0
Observed Loss132
Observed Complex0
Frequencyn/a


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