A curated catalogue of human genomic structural variation




Variant Details

Variant: essv40400



Internal ID10996512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:70896704..70962570hg38UCSC Ensembl
Innerchr5:70192531..70258397hg19UCSC Ensembl
Innerchr5:70228287..70294153hg18UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3865867
hg1965867
hg1865867
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv21413
Supporting Variants
SamplesNA12878
Known GenesSERF1A, SERF1B, SMN1, SMN2
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)essv40400
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