A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893206



Internal ID19184026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40835684..40857992hg38UCSC Ensembl
Outerchr19:40835684..40859190hg38UCSC Ensembl
Innerchr19:41341589..41363897hg19UCSC Ensembl
Outerchr19:41341589..41365095hg19UCSC Ensembl
Innerchr19:46033429..46055737hg18UCSC Ensembl
Outerchr19:46033429..46056935hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3823507
hg1923507
hg1823507
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797020, essv25788071, essv25796638
Samples
Known GenesCYP2A6
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893206
Frequency
Sample Size3017
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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