A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788273



Internal ID19160324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:55725823..55798457hg38UCSC Ensembl
Innerchr14:56192541..56265175hg19UCSC Ensembl
Innerchr14:55262294..55334928hg18UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3872635
hg1972635
hg1872635
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=23
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788273
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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