A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899428



Internal ID16193384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40848724..40886980hg38UCSC Ensembl
Innerchr19:41354629..41392885hg19UCSC Ensembl
Innerchr19:46046469..46084725hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3838257
hg1938257
hg1838257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579548
Supporting Variants
Samples
Known GenesCYP2A6, CYP2A7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899428
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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