A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579584



Internal ID16366993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40857396..40877894hg38UCSC Ensembl
Innerchr19:41363301..41383799hg19UCSC Ensembl
Innerchr19:46055141..46075639hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3820499
hg1920499
hg1820499
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6449n54
Supporting Variantsnssv899500, nssv899501
Samples
Known GenesCYP2A7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579584
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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