A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696213



Internal ID15432865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76163993..76179651hg38UCSC Ensembl
Innerchr11:75875037..75890695hg19UCSC Ensembl
Innerchr11:75552685..75568343hg18UCSC Ensembl
Innerchr11:75552685..75568343hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3815659
hg1915659
hg1815659
hg1715659
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518763
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696213
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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