A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788071



Internal ID19161591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40835684..40859190hg38UCSC Ensembl
Innerchr19:41341589..41365095hg19UCSC Ensembl
Innerchr19:46033429..46056935hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3823507
hg1923507
hg1823507
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893206
Supporting Variants
Samples
Known GenesCYP2A6
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788071
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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