A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659854



Internal ID15049820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4140066..4271051hg38UCSC Ensembl
Innerchr3:4181750..4312735hg19UCSC Ensembl
Innerchr3:4156750..4287735hg18UCSC Ensembl
Innerchr3:4156750..4287735hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38130986
hg19130986
hg18130986
hg17130986
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)nssv659854
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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