A curated catalogue of human genomic structural variation




Variant Details

Variant: essv42799



Internal ID11010849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50110579..50152433hg38UCSC Ensembl
Innerchr10:47926481..47966903hg19UCSC Ensembl
Innerchr10:47446487..47486909hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3841855
hg1940423
hg1840423
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv16990
Supporting Variants
SamplesNA18909
Known GenesFAM21B
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)essv42799
Frequency
Sample Size40
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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