A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787860



Internal ID19180952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:55718783..55795691hg38UCSC Ensembl
Innerchr14:56185501..56262409hg19UCSC Ensembl
Innerchr14:55255254..55332162hg18UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3876909
hg1976909
hg1876909
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892549
Supporting Variants
Samples
Known GenesLINC00520, RPL13AP3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=24
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787860
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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