A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3534n100



Internal ID22789621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40839241..40863792hg38UCSC Ensembl
chr19:41345146..41369697hg19UCSC Ensembl
chr19:46036986..46061537hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3824552
hg1924552
hg1824552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062739, nsv1062605
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)dgv3534n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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