A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579546



Internal ID16366955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40848724..40875635hg38UCSC Ensembl
Innerchr19:41354629..41381540hg19UCSC Ensembl
Innerchr19:46046469..46073380hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3826912
hg1926912
hg1826912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6446n54
Supporting Variantsnssv899417
Samples
Known GenesCYP2A6, CYP2A7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579546
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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