A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792178



Internal ID19179878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18223945..18537665hg38UCSC Ensembl
Innerchr14:19000422..19314142hg19UCSC Ensembl
Innerchr14:18070422..18384142hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38313721
hg19313721
hg18313721
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892456
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=82
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792178
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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