A curated catalogue of human genomic structural variation




Variant Details

Variant: essv67526



Internal ID11352937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:122656144..122657523hg38UCSC Ensembl
Innerchr12:123140691..123142070hg19UCSC Ensembl
Innerchr12:121706644..121708023hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381380
hg191380
hg181380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv15230
Supporting Variants
SamplesNA18858
Known Genes
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)essv67526
Frequency
Sample Size40
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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