A curated catalogue of human genomic structural variation




Variant Details

Variant: esv25599



Internal ID11042832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:23344687..23349736hg38UCSC Ensembl
Innerchr8:23202200..23207249hg19UCSC Ensembl
Innerchr8:23258145..23263194hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg385050
hg195050
hg185050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv15801
SamplesNA18523
Known GenesLOC100507156, LOXL2
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)esv25599
Frequency
Sample Size40
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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