A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29945



Internal ID11047468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73534947..73577725hg38UCSC Ensembl
Innerchr14:74001651..74044429hg19UCSC Ensembl
Innerchr14:73071404..73114182hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3842779
hg1942779
hg1842779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84184
SamplesWATSON
Known GenesACOT1, ACOT2, HEATR4
MethodOligo aCGH
AnalysisThe data were analyzed using the CGH Analytics software.
PlatformAgilent-014584 Human Genome 244K CGH Microarray (Alpha Test)
Comments
ReferenceWheeler_et_al_2008
Pubmed ID18421352
Accession Number(s)esv29945
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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