A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788174



Internal ID18832394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186062188..186212421hg38UCSC Ensembl
Innerchr4:186983342..187133575hg19UCSC Ensembl
Innerchr4:187220336..187370569hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38150234
hg19150234
hg18150234
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=53
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788174
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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