A curated catalogue of human genomic structural variation




Variant Details

Variant: essv51202



Internal ID11327162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:61468158..61474769hg38UCSC Ensembl
Innerchr8:62380717..62387328hg19UCSC Ensembl
Innerchr8:62543271..62549882hg18UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg386612
hg196612
hg186612
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv14468
Supporting Variants
SamplesNA11931
Known GenesCLVS1
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)essv51202
Frequency
Sample Size40
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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