A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697328



Internal ID15433980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65210448..65221591hg38UCSC Ensembl
Innerchr3:65196123..65207266hg19UCSC Ensembl
Innerchr3:65171163..65182306hg18UCSC Ensembl
Innerchr3:65171163..65182306hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3811144
hg1911144
hg1811144
hg1711144
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)nssv697328
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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