A curated catalogue of human genomic structural variation




Variant Details

Variant: esv16194



Internal ID11380113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1857835..1858485hg38UCSC Ensembl
Innerchr5:1857949..1858599hg19UCSC Ensembl
Innerchr5:1910949..1911599hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38651
hg19651
hg18651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv21624
Supporting Variantsessv53444, essv48124, essv50573, essv84134, essv38429, essv65452, essv37052, essv63058, essv82109, essv54874, essv34954, essv74127, essv41625
SamplesNA18502, NA18861, NA18508, NA19190, NA12156, NA19114, NA11894, NA15510, NA19099, NA19257, NA18517, NA19240, NA18505
Known Genes
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)esv16194
Frequency
Sample Size40
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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