A curated catalogue of human genomic structural variation




Variant Details

Variant: esv18938



Internal ID11036172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:3882544..3937944hg38UCSC Ensembl
InnerchrX:3800585..3855985hg19UCSC Ensembl
InnerchrX:3810585..3865985hg18UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3855401
hg1955401
hg1855401
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv22025
Supporting Variantsessv66265, essv41426, essv57466
SamplesNA11993, NA19240, NA18505
Known Genes
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)esv18938
Frequency
Sample Size40
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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