A curated catalogue of human genomic structural variation




Variant Details

Variant: esv26698



Internal ID11043931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84396593..84398062hg38UCSC Ensembl
Innerchr16:84430199..84431668hg19UCSC Ensembl
Innerchr16:82987700..82989169hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg381470
hg191470
hg181470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv16114
SamplesNA19129
Known GenesATP2C2
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)esv26698
Frequency
Sample Size40
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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