A curated catalogue of human genomic structural variation

Variant Details

Variant: esv29137

Internal ID11046370
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132148842..132150797hg38UCSC Ensembl
Innerchr12:132633387..132635342hg19UCSC Ensembl
Innerchr12:131199340..131201295hg18UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv11616
SamplesNA07037, NA18523, NA11931, NA12828, NA18517, NA12776, NA18505, NA18508, NA12004, NA11995, NA19190, NA12006, NA07045, NA06985, NA18907, NA12749
Known GenesNOC4L
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
Pubmed ID19812545
Accession Number(s)esv29137
Sample Size40
Observed Gain1
Observed Loss15
Observed Complex0

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