A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626860



Internal ID7013690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75752744..75756932hg38UCSC Ensembl
Innerchr11:75752761..75756916hg38UCSC Ensembl
Outerchr11:75752728..75756949hg38UCSC Ensembl
chr11:75463789..75467977hg19UCSC Ensembl
Innerchr11:75463806..75467961hg19UCSC Ensembl
Outerchr11:75463773..75467994hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg384189
hg194189
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14214063, essv14214052, essv14214071, essv14214070, essv14214062, essv14214060, essv14214053, essv14214050, essv14214056, essv14214065, essv14214066, essv14214057, essv14214059, essv14214055, essv14214061, essv14214069, essv14214064, essv14214068, essv14214051, essv14214054, essv14214058, essv14214067
SamplesNA18502, NA18486, HG03297, HG02888, HG03086, HG02620, HG03224, HG03520, HG02634, NA20318, HG02819, NA19210, HG02678, HG03311, HG03136, HG02635, HG03567, HG03433, HG03279, NA18876, NA19146, NA19431
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626860
Frequency
Sample Size2504
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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