A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520534



Internal ID15447827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:66391341..66400358hg38UCSC Ensembl
Innerchr1:66857024..66866041hg19UCSC Ensembl
Innerchr1:66629612..66638629hg18UCSC Ensembl
Innerchr1:66569045..66578062hg17UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg389018
hg199018
hg189018
hg179018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697473
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520534
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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