A curated catalogue of human genomic structural variation




Variant Details

Variant: essv58594



Internal ID11016045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105895678..106011758hg38UCSC Ensembl
Innerchr14:106361536..106477944hg19UCSC Ensembl
Innerchr14:105432581..105548989hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38116081
hg19116409
hg18116409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv13226
Supporting Variants
SamplesNA19108
Known GenesADAM6, KIAA0125
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)essv58594
Frequency
Sample Size40
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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