A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787326



Internal ID19172294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40850149..40878673hg38UCSC Ensembl
Innerchr19:41356054..41384578hg19UCSC Ensembl
Innerchr19:46047894..46076418hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3828525
hg1928525
hg1828525
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893202
Supporting Variants
Samples
Known GenesCYP2A6, CYP2A7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787326
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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