A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893205



Internal ID19184025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40844134..40850094hg38UCSC Ensembl
Outerchr19:40843869..40850594hg38UCSC Ensembl
Innerchr19:41350039..41355999hg19UCSC Ensembl
Outerchr19:41349774..41356499hg19UCSC Ensembl
Innerchr19:46041879..46047839hg18UCSC Ensembl
Outerchr19:46041614..46048339hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg386726
hg196726
hg186726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799527, essv25780679, essv25783389, essv25801619, essv25781285, essv25787479, essv25783183, essv25782616, essv25784687, essv25785028, essv25783840
Samples
Known GenesCYP2A6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893205
Frequency
Sample Size3017
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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