A curated catalogue of human genomic structural variation




Variant Details

Variant: essv81405



Internal ID11363748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:74891981..74918438hg38UCSC Ensembl
Innerchr7:74308100..74333471hg19UCSC Ensembl
Innerchr7:73946036..73971407hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3826458
hg1925372
hg1825372
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv11977
Supporting Variants
SamplesNA19114
Known GenesPMS2P5
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)essv81405
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