A curated catalogue of human genomic structural variation




Variant Details

Variant: essv37997



Internal ID11026230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:49529312..49605052hg38UCSC Ensembl
InnerchrX:49293915..49369655hg19UCSC Ensembl
InnerchrX:49180859..49256599hg18UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3875741
hg1975741
hg1875741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv15384
Supporting Variants
SamplesNA19257
Known GenesGAGE1, GAGE12B, GAGE12C, GAGE12D, GAGE12E, GAGE12F, GAGE12G, GAGE12H, GAGE12I, GAGE2A, GAGE2C, GAGE2E, GAGE6, GAGE8
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)essv37997
Frequency
Sample Size40
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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