A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894016



Internal ID19184870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:118847443..118954337hg38UCSC Ensembl
Outerchr4:118847443..118954337hg38UCSC Ensembl
Innerchr4:119768598..119875492hg19UCSC Ensembl
Outerchr4:119768598..119875492hg19UCSC Ensembl
Innerchr4:119988046..120094940hg18UCSC Ensembl
Outerchr4:119988046..120094940hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38106895
hg19106895
hg18106895
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787872
Samples
Known GenesSYNPO2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894016
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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