A curated catalogue of human genomic structural variation




Variant Details

Variant: esv18535



Internal ID11035769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8214782..8230370hg38UCSC Ensembl
Innerchr8:8072304..8087892hg19UCSC Ensembl
Innerchr8:8109714..8125302hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3815589
hg1915589
hg1815589
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv25631
Supporting Variantsessv59939, essv66159, essv82386
SamplesNA18523, NA19114, NA19240
Known GenesFAM86B3P
MethodOligo aCGH
AnalysisSegment log2 ratios from each sample. This was done running the GADA algorithm (Pique-Regi et al., 2008) using the options "-M 10 -T 10 -a 2.5". Filter non-CNV segments using intensity thresholds. Merge remaining CNV "calls" within each sample. Adjacent calls of the same direction (gain or loss) are merged if both: the distance between calls is less than 10kb, and the distance between calls is less than 10% of the size of the largest of the two calls.
PlatformSanger H. Sapiens 42mCGH Array 5781_53 726K v1
Comments
ReferenceConrad_et_al_2009
Pubmed ID19812545
Accession Number(s)esv18535
Frequency
Sample Size40
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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