A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788018



Internal ID18830697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186011626..186201164hg38UCSC Ensembl
Innerchr4:186932780..187122318hg19UCSC Ensembl
Innerchr4:187169774..187359312hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38189539
hg19189539
hg18189539
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894090
Supporting Variants
Samples
Known GenesCYP4V2, FAM149A, FLJ38576, TLR3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=59
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788018
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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