A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787973



Internal ID19180139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:43061086..43477886hg38UCSC Ensembl
Innerchr14:43530289..43947089hg19UCSC Ensembl
Innerchr14:42600039..43016839hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38416801
hg19416801
hg18416801
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892523
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=37
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787973
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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