A curated catalogue of human genomic structural variation




Variant Details

Variant: esv21978



Internal ID4352879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:16974284..16976716hg38UCSC Ensembl
Innerchr10:17016283..17018715hg19UCSC Ensembl
Innerchr10:17056289..17058721hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382433
hg192433
hg182433
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv17505
SamplesNA19114
Known GenesCUBN
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)esv21978
Frequency
Sample Size40
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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