A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652121



Internal ID15388773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22990516..22990849hg38UCSC Ensembl
Innerchr3:23032007..23032340hg19UCSC Ensembl
Innerchr3:23007011..23007344hg18UCSC Ensembl
Innerchr3:23007011..23007344hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38334
hg19334
hg18334
hg17334
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517473
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv652121
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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