A curated catalogue of human genomic structural variation




Variant Details

Variant: essv33721



Internal ID10999505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15129647..15134512hg38UCSC Ensembl
Innerchr1:15456143..15461008hg19UCSC Ensembl
Innerchr1:15328730..15333595hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg384866
hg194866
hg184866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv15067
Supporting Variants
SamplesNA18502
Known GenesTMEM51-AS1
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)essv33721
Frequency
Sample Size40
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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