A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29955



Internal ID11394164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105545378..105749141hg38UCSC Ensembl
Innerchr14:106011715..106215478hg19UCSC Ensembl
Innerchr14:105082760..105286523hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38203764
hg19203764
hg18203764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84194
SamplesWATSON
Known GenesELK2AP, MIR8071-1, MIR8071-2
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)esv29955
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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