A curated catalogue of human genomic structural variation




Variant Details

Variant: essv61136



Internal ID10988540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:1251692..1325062hg38UCSC Ensembl
InnerchrX:1370585..1443955hg19UCSC Ensembl
InnerchrX:1330585..1403955hg18UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3873371
hg1973371
hg1873371
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv16136
Supporting Variants
SamplesNA12239
Known GenesCSF2RA, MIR3690, MIR3690-2
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)essv61136
Frequency
Sample Size40
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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