A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3569427



Internal ID18867708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40846466..40886980hg38UCSC Ensembl
Innerchr19:41352371..41392885hg19UCSC Ensembl
Innerchr19:46044211..46084725hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3840515
hg1940515
hg1840515
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056372
Supporting Variants
Samples
Known GenesCYP2A6, CYP2A7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3569427
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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