A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579529



Internal ID16366938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40844134..40866570hg38UCSC Ensembl
Innerchr19:41350039..41372475hg19UCSC Ensembl
Innerchr19:46041879..46064315hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3822437
hg1922437
hg1822437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6444n54
Supporting Variantsnssv899393
Samples
Known GenesCYP2A6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579529
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer