A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892561



Internal ID18836695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73365865..73620531hg38UCSC Ensembl
Outerchr14:73365865..73620531hg38UCSC Ensembl
Innerchr14:73832573..74087235hg19UCSC Ensembl
Outerchr14:73832573..74087235hg19UCSC Ensembl
Innerchr14:72902326..73156988hg18UCSC Ensembl
Outerchr14:72902326..73156988hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38254667
hg19254663
hg18254663
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792504
Samples
Known GenesACOT1, ACOT2, ACOT4, ACOT6, C14orf169, HEATR4, NUMB
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892561
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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