A curated catalogue of human genomic structural variation




Variant Details

Variant: essv66805



Internal ID11341670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178921630..178925782hg38UCSC Ensembl
Innerchr5:178348631..178352783hg19UCSC Ensembl
Innerchr5:178281237..178285389hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg384153
hg194153
hg184153
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv12223
Supporting Variants
SamplesNA12828
Known GenesZFP2
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)essv66805
Frequency
Sample Size40
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer