A curated catalogue of human genomic structural variation




Variant Details

Variant: esv26695



Internal ID11043928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:146906705..146909144hg38UCSC Ensembl
Innerchr5:146286268..146288707hg19UCSC Ensembl
Innerchr5:146266461..146268900hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382440
hg192440
hg182440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv12990, esv14063, esv12190
SamplesNA12489, NA19108, NA18505, NA18508, NA18916, NA19190, NA07045, NA19129, NA18907, NA19225
Known GenesPPP2R2B
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)esv26695
Frequency
Sample Size40
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer