A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570859



Internal ID16011582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101488263..101764677hg38UCSC Ensembl
Innerchr15:102028468..102304880hg19UCSC Ensembl
Innerchr15:99845991..100122403hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38276415
hg19276413
hg18276413
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4792n54
Supporting Variantsnssv851083
Samples
Known GenesPCSK6, TARSL2, TM2D3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570859
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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