A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3535n100



Internal ID22789622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40839241..40865028hg38UCSC Ensembl
chr19:41345146..41370933hg19UCSC Ensembl
chr19:46036986..46062773hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3825788
hg1925788
hg1825788
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066928, nsv1058924, nsv1059052
Samples
Known GenesCYP2A6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3535n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss6
Observed Complex0
Frequencyn/a


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