A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653686



Internal ID15043652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69151376..69244456hg38UCSC Ensembl
Innerchr15:69443715..69536795hg19UCSC Ensembl
Innerchr15:67230769..67323849hg18UCSC Ensembl
Innerchr15:67230769..67323849hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3893081
hg1993081
hg1893081
hg1793081
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517185
Supporting Variants
Samples
Known GenesGLCE, MIR548H4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653686
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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