A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525863



Internal ID15453156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27202697..27222139hg38UCSC Ensembl
Innerchr15:27447844..27467286hg19UCSC Ensembl
Innerchr15:25030590..25050032hg18UCSC Ensembl
Innerchr15:25030590..25050032hg17UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3819443
hg1919443
hg1819443
hg1719443
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702060
Samples
Known GenesGABRG3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525863
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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