A curated catalogue of human genomic structural variation




Variant Details

Variant: esv23563



Internal ID11040796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7212338..7224109hg38UCSC Ensembl
Innerchr4:7214065..7225836hg19UCSC Ensembl
Innerchr4:7264966..7276737hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3811772
hg1911772
hg1811772
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv11868, esv19322
SamplesNA11995, NA12004, NA11993, NA18909, NA19108, NA12749, NA12006
Known GenesSORCS2
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)esv23563
Frequency
Sample Size40
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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