A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3540n100



Internal ID22789627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40846466..40893982hg38UCSC Ensembl
chr19:41352371..41399887hg19UCSC Ensembl
chr19:46044211..46091727hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3847517
hg1947517
hg1847517
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063860, nsv1056284, nsv1056372
Samples
Known GenesCYP2A6, CYP2A7, CYP2G1P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3540n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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