A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797941



Internal ID19160228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105581568..105708865hg38UCSC Ensembl
Innerchr14:106047905..106175202hg19UCSC Ensembl
Innerchr14:105118950..105246247hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38127298
hg19127298
hg18127298
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892587
Supporting Variants
Samples
Known GenesELK2AP, MIR8071-1, MIR8071-2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797941
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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