A curated catalogue of human genomic structural variation

Variant Details

Variant: esv19409

Internal ID11036643
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14688324..14771151hg38UCSC Ensembl
Innerchr16:14782181..14865008hg19UCSC Ensembl
Innerchr16:14689682..14772509hg18UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv28787
Supporting Variantsessv60507, essv46643, essv84120, essv33144, essv72766, essv35235, essv81732, essv33773, essv67839, essv47019, essv62137, essv50119
SamplesNA18861, NA18523, NA19114, NA18517, NA19147, NA19190, NA12239, NA19129, NA18502, NA18858, NA18907, NA19225
Known GenesNPIPA2, NPIPA3, PLA2G10
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
Pubmed ID19812545
Accession Number(s)esv19409
Sample Size40
Observed Gain12
Observed Loss0
Observed Complex0

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