A curated catalogue of human genomic structural variation




Variant Details

Variant: esv13146



Internal ID11377065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84491321..84518103hg38UCSC Ensembl
Innerchr15:85034506..85061334hg19UCSC Ensembl
Innerchr15:82835510..82862338hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3826783
hg1926829
hg1826829
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv29772
Supporting Variantsessv68227, essv83684, essv61366, essv71031
SamplesNA19190, NA18916, NA12239, NA18858
Known GenesDNM1P41, GOLGA6L5P
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)esv13146
Frequency
Sample Size40
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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