A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758564



Internal ID9634023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:10083096..10263971hg38UCSC Ensembl
InnerchrX:10051136..10232011hg19UCSC Ensembl
InnerchrX:10011136..10192011hg18UCSC Ensembl
InnerchrX:9860872..10041747hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38180876
hg19180876
hg18180876
hg17180876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2758861
Supporting Variantsessv19587
SamplesNA12864
Known GenesCLCN4, WWC3
MethodBAC aCGH
AnalysisArray images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
PlatformAgilent
Comments
ReferenceRedon_et_al_2006
Pubmed ID17122850
Accession Number(s)esv2758564
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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