A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690683



Internal ID15080649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4227212..4231805hg38UCSC Ensembl
Innerchr3:4268896..4273489hg19UCSC Ensembl
Innerchr3:4243896..4248489hg18UCSC Ensembl
Innerchr3:4243896..4248489hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg384594
hg194594
hg184594
hg174594
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516589
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690683
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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