A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29947



Internal ID11047470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38963107..38989480hg38UCSC Ensembl
Innerchr22:39359112..39385485hg19UCSC Ensembl
Innerchr22:37689058..37715431hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3826374
hg1926374
hg1826374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84186
SamplesWATSON
Known GenesAPOBEC3A, APOBEC3A_B, APOBEC3B
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)esv29947
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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