A curated catalogue of human genomic structural variation




Variant Details

Variant: esv20684



Internal ID11037918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:71004138..71095553hg38UCSC Ensembl
Innerchr5:70299965..70391380hg19UCSC Ensembl
Innerchr5:70335721..70427136hg18UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3891416
hg1991416
hg1891416
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv22113
Supporting Variantsessv46750, essv37851, essv51415, essv36141, essv53023, essv77329, essv68567, essv40938, essv76357, essv70941, essv75225
SamplesNA18861, NA18508, NA12414, NA11931, NA12004, NA18916, NA12878, NA18907, NA19257, NA18858, NA18511
Known GenesGTF2H2, GTF2H2B, GTF2H2C, GTF2H2D, LOC647859, NAIP
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)esv20684
Frequency
Sample Size40
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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