A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3577244



Internal ID18358756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:124452691..124455890hg38UCSC Ensembl
InnerchrX:123586541..123589740hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9830316
Samples401251WN
Known GenesTENM1
MethodSNP array
AnalysisWe used four separate algorithms to detect CNVs; Affymetrix Chromosome Analysis Suite (ChAS), iPattern, Nexus and Partek. Our primary analysis was performed based on ChAS CNV calls, which were then supported using the remaining three algorithms to construct a confidence set of CNVs. For all algorithms, we have used 8 probes and >1kb as a base line cutoff for CNV detection.
PlatformAffymetrix CytoScan HD 2.7M array
Comments
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)esv3577244
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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