A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899500



Internal ID16193456
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 StatusS
Merged Variantsnsv579584
Supporting Variants
Samples
Known GenesCYP2A7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899500
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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