A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796638



Internal ID19176233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40835684..40859189hg38UCSC Ensembl
Innerchr19:41341589..41365094hg19UCSC Ensembl
Innerchr19:46033429..46056934hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3823506
hg1923506
hg1823506
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893206
Supporting Variants
Samples
Known GenesCYP2A6
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796638
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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