A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663790



Internal ID9929895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50026295..50026515hg38UCSC Ensembl
chr22:50464724..50464944hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6469092, essv6551651, essv6309890, essv5951930, essv6572804, essv5704505, essv5490577, essv5904750, essv6374693, essv6229938, essv5831526, essv6007388, essv6011749, essv5601844, essv5471580, essv6480042, essv5944340, essv6133108, essv6177720, essv5583383, essv6559996, essv5644315, essv6014834, essv6018055, essv5508937, essv6059035, essv6483019, essv6321253, essv5890926, essv6051239, essv6593371, essv6339737, essv6067499, essv6038201, essv5704963, essv6442468, essv6385102, essv6435902, essv5622993, essv6053889, essv5448140, essv6235689, essv6371024, essv6200971, essv6220840, essv6347299, essv6593240, essv5996240, essv5908382, essv5689279, essv5573352, essv5975710, essv6451106, essv6415291, essv5988017, essv5539787, essv5399746, essv6540720, essv6426253, essv5716173, essv6306956, essv6529685, essv6409591, essv6440804, essv6112731, essv5985213, essv5498359, essv5769177, essv6230849, essv5784164, essv5612647, essv6541672, essv5437636, essv5715205, essv6133951, essv5698833, essv5834963, essv6136690, essv5708838, essv5458673, essv5967100, essv5554666, essv5437249, essv6532237, essv5675984, essv6117359, essv6465288, essv6229039, essv5750008, essv6575455, essv6545863, essv6363417, essv6156245, essv6475165, essv5549289, essv5892254, essv6231434, essv6401003, essv6059886, essv5840123
SamplesHG01060, NA12717, HG01173, HG00671, HG01079, HG00315, HG00318, HG00699, HG01456, NA07357, HG00693, HG00327, HG00271, HG00663, NA19374, NA19381, HG01366, HG01070, HG00251, HG01351, HG00689, NA19198, HG00330, NA19404, NA11930, HG00281, HG00139, HG00277, HG01080, HG01067, HG00683, HG00335, HG00325, HG00232, HG00309, HG00338, HG00326, HG00323, HG00253, HG00464, HG00260, HG00313, HG00137, HG01183, HG00268, HG01171, HG00282, HG00557, HG00328, HG00428, HG00701, HG00657, HG00320, HG00583, HG00344, HG00500, HG00263, HG00275, HG00708, HG01390, NA18566, HG00324, HG00284, HG01073, NA12829, HG01383, HG00140, HG01334, HG00276, HG00246, HG01107, NA18546, NA18632, HG00254, NA19390, NA18559, HG00375, HG00278, NA19380, HG01174, HG00473, HG00237, HG00319, HG01108, NA19360, HG00339, HG00125, HG00672, HG00111, HG00421, HG00342, NA18636, HG00698, HG00280, HG00343, HG00252, HG01378, HG01082, HG00345, NA18622
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663790
Frequency
Sample Size1151
Observed Gain0
Observed Loss100
Observed Complex0
Frequencyn/a


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