A curated catalogue of human genomic structural variation




Variant Details

Variant: esv15812



Internal ID11033046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12780465..13050020hg38UCSC Ensembl
Innerchr1:12840608..13052938hg19UCSC Ensembl
Innerchr1:12763195..12975525hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38269556
hg19212331
hg18212331
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv28644
Supporting Variantsessv75263, essv49683, essv76255, essv61072, essv36576, essv47188
SamplesNA18861, NA12414, NA12004, NA11894, NA12239, NA18517
Known GenesHNRNPCL1, LOC649330, PRAMEF1, PRAMEF10, PRAMEF11, PRAMEF2, PRAMEF22, PRAMEF4, PRAMEF6, PRAMEF7, PRAMEF8
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)esv15812
Frequency
Sample Size40
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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