A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788015



Internal ID19182893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40844990..40873243hg38UCSC Ensembl
Innerchr19:41350895..41379148hg19UCSC Ensembl
Innerchr19:46042735..46070988hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3828254
hg1928254
hg1828254
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893202
Supporting Variants
Samples
Known GenesCYP2A6
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788015
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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