A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704810



Internal ID15441462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:15563569..15607720hg38UCSC Ensembl
Innerchr21:16935888..16980039hg19UCSC Ensembl
Innerchr21:15857759..15901910hg18UCSC Ensembl
Innerchr21:15857759..15901910hg17UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3844152
hg1944152
hg1844152
hg1744152
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528246
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704810
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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