A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699797



Internal ID15436449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:191938624..191941554hg38UCSC Ensembl
Innerchr3:191656413..191659343hg19UCSC Ensembl
Innerchr3:193139107..193142037hg18UCSC Ensembl
Innerchr3:193139115..193142045hg17UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg382931
hg192931
hg182931
hg172931
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517535
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699797
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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