A curated catalogue of human genomic structural variation




Variant Details

Variant: essv44887



Internal ID10992163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7712279..7774739hg38UCSC Ensembl
Innerchr8:7569801..7632261hg19UCSC Ensembl
Innerchr8:7607211..7669671hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3862461
hg1962461
hg1862461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv16077
Supporting Variants
SamplesNA12489
Known GenesFAM90A10P
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)essv44887
Frequency
Sample Size40
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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