A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694618



Internal ID15084584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:166076111..166096812hg38UCSC Ensembl
Innerchr3:165793899..165814600hg19UCSC Ensembl
Innerchr3:167276593..167297294hg18UCSC Ensembl
Innerchr3:167276601..167297302hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3820702
hg1920702
hg1820702
hg1720702
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520596
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694618
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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