A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579593



Internal ID16367002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40875596..40886585hg38UCSC Ensembl
Innerchr19:41381501..41392490hg19UCSC Ensembl
Innerchr19:46073341..46084330hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3810990
hg1910990
hg1810990
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6452n54
Supporting Variantsnssv899516
Samples
Known GenesCYP2A7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579593
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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