A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626810



Internal ID7013640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73175020..73185975hg38UCSC Ensembl
Innerchr11:73175057..73185938hg38UCSC Ensembl
Outerchr11:73174983..73186012hg38UCSC Ensembl
chr11:72886065..72897020hg19UCSC Ensembl
Innerchr11:72886102..72896983hg19UCSC Ensembl
Outerchr11:72886028..72897057hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3810956
hg1910956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14212062, essv14212063
SamplesNA20882, NA20900
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626810
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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