A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792504



Internal ID18834078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73365865..73620531hg38UCSC Ensembl
Innerchr14:73832573..74087235hg19UCSC Ensembl
Innerchr14:72902326..73156988hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38254667
hg19254663
hg18254663
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892561
Supporting Variants
Samples
Known GenesACOT1, ACOT2, ACOT4, ACOT6, C14orf169, HEATR4, NUMB
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=32
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792504
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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