A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683952



Internal ID15420604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:42618138..42623932hg38UCSC Ensembl
Innerchr21:44038248..44044042hg19UCSC Ensembl
Innerchr21:42911317..42917111hg18UCSC Ensembl
Innerchr21:42911317..42917111hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg385795
hg195795
hg185795
hg175795
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521182
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683952
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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