A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519166



Internal ID15446459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:74707562..74722672hg38UCSC Ensembl
Innerchr13:75281699..75296809hg19UCSC Ensembl
Innerchr13:74179700..74194810hg18UCSC Ensembl
Innerchr13:74179700..74194810hg17UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3815111
hg1915111
hg1815111
hg1715111
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696649
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519166
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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