A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659573



Internal ID15396225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101788321..101826646hg38UCSC Ensembl
Innerchr15:102328524..102366849hg19UCSC Ensembl
Innerchr15:100146047..100184372hg18UCSC Ensembl
Innerchr15:100146047..100184372hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3838326
hg1938326
hg1838326
hg1738326
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519940
Supporting Variants
Samples
Known GenesOR4F15, OR4F6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659573
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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