A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3574431



Internal ID18702629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:120155012..120156379hg38UCSC Ensembl
InnerchrX:119288918..119290285hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg381368
hg191368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2397e212
Supporting Variantsessv9829800, essv9829798, essv9829797, essv9829796, essv9829794, essv9829793, essv9829795
Samples400927BD, 401385BB, 400199SA, 400425SL, 401064FR, 400615RI, 401580CA
Known Genes
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)esv3574431
Frequency
Sample Size873
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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