A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899429



Internal ID16193385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40848724..40887855hg38UCSC Ensembl
Innerchr19:41354629..41393760hg19UCSC Ensembl
Innerchr19:46046469..46085600hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3839132
hg1939132
hg1839132
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579549
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)nssv899429
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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