A curated catalogue of human genomic structural variation




Variant Details

Variant: esv10145



Internal ID11374064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31317869..31333843hg38UCSC Ensembl
Innerchr6:31285646..31301620hg19UCSC Ensembl
Innerchr6:31393625..31409599hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3815975
hg1915975
hg1815975
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv27315
Supporting Variantsessv57663, essv65154, essv56129, essv66751, essv59846, essv77634, essv83150, essv74052, essv82345, essv49369, essv46037, essv39049, essv58758, essv38496, essv79673, essv68011, essv70747, essv41319, essv32561, essv62885, essv64282
SamplesNA19190, NA18916, NA12287, NA12156, NA12828, NA11993, NA07045, NA19114, NA15510, NA19257, NA06985, NA18523, NA18858, NA19108, NA19147, NA18517, NA19240, NA12749, NA18505, NA19129, NA12776
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)esv10145
Frequency
Sample Size40
Observed Gain21
Observed Loss0
Observed Complex0
Frequencyn/a


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