A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661475



Internal ID15398127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65207571..65225745hg38UCSC Ensembl
Innerchr3:65193246..65211420hg19UCSC Ensembl
Innerchr3:65168286..65186460hg18UCSC Ensembl
Innerchr3:65168286..65186460hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3818175
hg1918175
hg1818175
hg1718175
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)nssv661475
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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