A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686404



Internal ID15423056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65206172..65226921hg38UCSC Ensembl
Innerchr3:65191847..65212596hg19UCSC Ensembl
Innerchr3:65166887..65187636hg18UCSC Ensembl
Innerchr3:65166887..65187636hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3820750
hg1920750
hg1820750
hg1720750
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516641
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686404
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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