A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579545



Internal ID16366954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40848724..40875596hg38UCSC Ensembl
Innerchr19:41354629..41381501hg19UCSC Ensembl
Innerchr19:46046469..46073341hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3826873
hg1926873
hg1826873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899416
Samples
Known GenesCYP2A6, CYP2A7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579545
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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