A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698134



Internal ID15434786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:15101837..15110322hg38UCSC Ensembl
Innerchr21:16474158..16482643hg19UCSC Ensembl
Innerchr21:15396029..15404514hg18UCSC Ensembl
Innerchr21:15396029..15404514hg17UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg388486
hg198486
hg188486
hg178486
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521517
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698134
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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