A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682932



Internal ID15419584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145507323..145536355hg38UCSC Ensembl
Innerchr3:145225110..145254142hg19UCSC Ensembl
Innerchr3:146707800..146736832hg18UCSC Ensembl
Innerchr3:146707808..146736840hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3829033
hg1929033
hg1829033
hg1729033
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520174
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682932
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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