A curated catalogue of human genomic structural variation




Variant Details

Variant: essv53697



Internal ID11348713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:13261812..13262992hg38UCSC Ensembl
Innerchr18:13261811..13262991hg19UCSC Ensembl
Innerchr18:13251811..13252991hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg381181
hg191181
hg181181
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv12934
Supporting Variants
SamplesNA18508
Known GenesLDLRAD4
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)essv53697
Frequency
Sample Size40
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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