A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657667



Internal ID15394319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13507020..13519826hg38UCSC Ensembl
Innerchr3:13548520..13561326hg19UCSC Ensembl
Innerchr3:13523520..13536326hg18UCSC Ensembl
Innerchr3:13523520..13536326hg17UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3812807
hg1912807
hg1812807
hg1712807
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519673
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657667
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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