A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521239



Internal ID15101846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:156037538..156044936hg38UCSC Ensembl
Innerchr3:155755327..155762725hg19UCSC Ensembl
Innerchr3:157238021..157245419hg18UCSC Ensembl
Innerchr3:157238029..157245427hg17UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg387399
hg197399
hg187399
hg177399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv687412, nssv688030, nssv689096
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521239
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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