A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694741



Internal ID15431393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72567429..72586431hg38UCSC Ensembl
Innerchr15:72859770..72878772hg19UCSC Ensembl
Innerchr15:70646824..70665826hg18UCSC Ensembl
Innerchr15:70646824..70665826hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3819003
hg1919003
hg1819003
hg1719003
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521972
Supporting Variants
Samples
Known GenesARIH1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694741
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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