A curated catalogue of human genomic structural variation




Variant Details

Variant: essv76712



Internal ID11003188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:236421051..236422232hg38UCSC Ensembl
Innerchr1:236584351..236585532hg19UCSC Ensembl
Innerchr1:234650974..234652155hg18UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg381182
hg191182
hg181182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv19151
Supporting Variants
SamplesNA18511
Known GenesEDARADD
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)essv76712
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