A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv851076



Internal ID16145032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101408007..101602444hg38UCSC Ensembl
Innerchr15:101948212..102142647hg19UCSC Ensembl
Innerchr15:99765735..99960170hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38194438
hg19194436
hg18194436
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570852
Supporting Variants
Samples
Known GenesPCSK6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv851076
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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