A curated catalogue of human genomic structural variation




Variant Details

Variant: esv13648



Internal ID11030882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:69987590..70129539hg38UCSC Ensembl
Innerchr5:69283417..69425366hg19UCSC Ensembl
Innerchr5:69319173..69461122hg18UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38141950
hg19141950
hg18141950
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv22113
Supporting Variantsessv71789, essv45277, essv49929, essv41153, essv67963, essv74941, essv43051
SamplesNA12004, NA19225, NA18858, NA18909, NA18517, NA18505, NA19129
Known GenesSERF1A, SERF1B, SMA4, 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)esv13648
Frequency
Sample Size40
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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