A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10034



Internal ID9607042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:42371195..42687300hg38UCSC Ensembl
Innerchr22:42767201..43083306hg19UCSC Ensembl
Innerchr22:41097145..41413250hg18UCSC Ensembl
Innerchr22:41091699..41407804hg17UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38316106
hg19316106
hg18316106
hg17316106
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758548
Supporting Variants
SamplesNA19099
Known GenesATP5L2, CYB5R3, NFAM1, POLDIP3, RNU12, RRP7A, RRP7B, SERHL, SERHL2
MethodBAC aCGH
AnalysisArray images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
PlatformAgilent
Comments
ReferenceRedon_et_al_2006
Pubmed ID17122850
Accession Number(s)essv10034
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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