A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3577135



Internal ID18358647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:116454112..116463757hg38UCSC Ensembl
InnerchrX:115585278..115594918hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg389646
hg199641
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2383e212
Supporting Variantsessv9829451, essv9829450
Samples401075MN, 400732MA
Known GenesCXorf61, SLC6A14
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)esv3577135
Frequency
Sample Size873
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer