A curated catalogue of human genomic structural variation




Variant Details

Variant: essv75362



Internal ID10984252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87111893..87214683hg38UCSC Ensembl
Innerchr10:88871650..88974440hg19UCSC Ensembl
Innerchr10:88861630..88964420hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38102791
hg19102791
hg18102791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv19607
Supporting Variants
SamplesNA12004
Known GenesFAM35A
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)essv75362
Frequency
Sample Size40
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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