A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9833671



Internal ID18654308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:150541636..150544244hg38UCSC Ensembl
InnerchrX:149710085..149712693hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg382609
hg192609
Variant TypeCNV gain
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3577524
Supporting Variants
Samples400818BL
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
CommentsNumber of probes=8
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9833671
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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