A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783389



Internal ID19177454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40844134..40850094hg38UCSC Ensembl
Innerchr19:41350039..41355999hg19UCSC Ensembl
Innerchr19:46041879..46047839hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg385961
hg195961
hg185961
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893205
Supporting Variants
Samples
Known GenesCYP2A6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783389
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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