A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687668



Internal ID15424320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:153356087..153368037hg38UCSC Ensembl
Innerchr3:153073876..153085826hg19UCSC Ensembl
Innerchr3:154556566..154568516hg18UCSC Ensembl
Innerchr3:154556574..154568524hg17UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3811951
hg1911951
hg1811951
hg1711951
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520682
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687668
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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