A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688344



Internal ID15424996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162412903..162485225hg38UCSC Ensembl
Innerchr3:162130691..162203013hg19UCSC Ensembl
Innerchr3:163613385..163685707hg18UCSC Ensembl
Innerchr3:163613393..163685715hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3872323
hg1972323
hg1872323
hg1772323
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516841
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688344
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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