A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626777



Internal ID7013607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71501694..71504680hg38UCSC Ensembl
Innerchr11:71501695..71504679hg38UCSC Ensembl
Outerchr11:71501693..71504681hg38UCSC Ensembl
chr11:71212740..71215726hg19UCSC Ensembl
Innerchr11:71212741..71215725hg19UCSC Ensembl
Outerchr11:71212739..71215727hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382987
hg192987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14210462, essv14210447, essv14210450, essv14210446, essv14210466, essv14210459, essv14210458, essv14210451, essv14210444, essv14210467, essv14210460, essv14210461, essv14210445, essv14210464, essv14210457, essv14210448, essv14210465, essv14210455, essv14210449, essv14210454, essv14210441, essv14210438, essv14210439, essv14210440, essv14210453, essv14210456, essv14210437, essv14210452, essv14210442, essv14210443, essv14210463
SamplesHG02614, HG03378, NA19920, HG03069, HG03079, HG02143, HG02315, HG02573, HG03212, NA19207, HG03380, HG01353, HG03547, HG02968, HG03085, HG02979, HG02635, HG02330, HG02282, HG03461, HG03539, HG02501, HG01894, HG03473, NA20348, HG03066, HG03063, HG03376, NA18511, HG03118, HG03196
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626777
Frequency
Sample Size2504
Observed Gain0
Observed Loss31
Observed Complex0
Frequencyn/a


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