A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524576



Internal ID15451869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:67472068..67480719hg38UCSC Ensembl
Innerchr1:67937751..67946402hg19UCSC Ensembl
Innerchr1:67710339..67718990hg18UCSC Ensembl
Innerchr1:67649772..67658423hg17UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg388652
hg198652
hg188652
hg178652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700532
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524576
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer