A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526342



Internal ID15106949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57273661..57305082hg38UCSC Ensembl
Innerchr15:57565859..57597280hg19UCSC Ensembl
Innerchr15:55353151..55384572hg18UCSC Ensembl
Innerchr15:55353151..55384572hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3831422
hg1931422
hg1831422
hg1731422
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702634
Samples
Known GenesLINC00926, TCF12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526342
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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