A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523732



Internal ID15451025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:54914266..54920054hg38UCSC Ensembl
Innerchr1:55379939..55385727hg19UCSC Ensembl
Innerchr1:55152527..55158315hg18UCSC Ensembl
Innerchr1:55091960..55097748hg17UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg385789
hg195789
hg185789
hg175789
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699548
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523732
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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