A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698765



Internal ID15435417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145670130..145764299hg38UCSC Ensembl
Innerchr3:145387917..145482086hg19UCSC Ensembl
Innerchr3:146870607..146964776hg18UCSC Ensembl
Innerchr3:146870615..146964784hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3894170
hg1994170
hg1894170
hg1794170
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523075
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698765
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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