A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520460



Internal ID15447753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:81608815..81618055hg38UCSC Ensembl
Innerchr1:82074500..82083740hg19UCSC Ensembl
Innerchr1:81847088..81856328hg18UCSC Ensembl
Innerchr1:81786521..81795761hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg389241
hg199241
hg189241
hg179241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697434
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520460
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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