A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698638



Internal ID15435290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41285260..41285621hg38UCSC Ensembl
Innerchr21:42657187..42657548hg19UCSC Ensembl
Innerchr21:41579057..41579418hg18UCSC Ensembl
Innerchr21:41579057..41579418hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38362
hg19362
hg18362
hg17362
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522968
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698638
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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