A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692838



Internal ID15082804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:50134964..50137453hg38UCSC Ensembl
Innerchr3:50172397..50174886hg19UCSC Ensembl
Innerchr3:50147401..50149890hg18UCSC Ensembl
Innerchr3:50147401..50149890hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382490
hg192490
hg182490
hg172490
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515986
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692838
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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