A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695536



Internal ID15432188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:31950507..31956217hg38UCSC Ensembl
Innerchr21:33322819..33328529hg19UCSC Ensembl
Innerchr21:32244690..32250400hg18UCSC Ensembl
Innerchr21:32244690..32250400hg17UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg385711
hg195711
hg185711
hg175711
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518119
Supporting Variants
Samples
Known GenesHUNK
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695536
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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