A curated catalogue of human genomic structural variation




Variant Details

Variant: esv13699



Internal ID11030933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12297564..12695622hg38UCSC Ensembl
Innerchr8:12155035..12553131hg19UCSC Ensembl
Innerchr8:12199406..12597502hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38398059
hg19398097
hg18398097
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv25198
Supporting Variantsessv34260, essv46850, essv67665, essv38003, essv49126, essv36391, essv61976
SamplesNA18502, NA18861, NA18907, NA12239, NA19257, NA18858, NA07037
Known GenesDEFB109P1, DEFB130, FAM66A, FAM86B2, FAM90A25P, LOC100133267, LOC100506990, LOC649352, LOC729732
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)esv13699
Frequency
Sample Size40
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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