A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659330



Internal ID15049296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69151725..69244456hg38UCSC Ensembl
Innerchr15:69444064..69536795hg19UCSC Ensembl
Innerchr15:67231118..67323849hg18UCSC Ensembl
Innerchr15:67231118..67323849hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3892732
hg1992732
hg1892732
hg1792732
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)nssv659330
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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