A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797928



Internal ID18814706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20889996..20925130hg38UCSC Ensembl
Innerchr14:21358155..21393289hg19UCSC Ensembl
Innerchr14:20427995..20463129hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3835135
hg1935135
hg1835135
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892467
Supporting Variants
Samples
Known GenesECRP, RNASE3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797928
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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