A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699931



Internal ID15089897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125943391..125955329hg38UCSC Ensembl
Innerchr11:125813286..125825224hg19UCSC Ensembl
Innerchr11:125318496..125330434hg18UCSC Ensembl
Innerchr11:125318496..125330434hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3811939
hg1911939
hg1811939
hg1711939
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516919
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699931
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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