A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv851216



Internal ID15798486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101733297..101948265hg38UCSC Ensembl
Innerchr15:102273500..102488468hg19UCSC Ensembl
Innerchr15:100091023..100305991hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38214969
hg19214969
hg18214969
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570911
Supporting Variants
Samples
Known GenesOR4F13P, OR4F15, OR4F4, OR4F6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv851216
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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