A curated catalogue of human genomic structural variation




Variant Details

Variant: essv74912



Internal ID11330222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74326520..74430368hg38UCSC Ensembl
Innerchr16:74360418..74464266hg19UCSC Ensembl
Innerchr16:72917919..73021767hg18UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg38103849
hg19103849
hg18103849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv10189
Supporting Variants
SamplesNA12004
Known GenesCLEC18B, LOC283922
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)essv74912
Frequency
Sample Size40
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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