A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3573749



Internal ID18355261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:31438334..31440703hg38UCSC Ensembl
InnerchrX:31456451..31458820hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg382370
hg192370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2251e212
Supporting Variantsessv9824872, essv9824877, essv9824873, essv9824870, essv9824875
Samples401039PA, 401652HL, 402023EC, 401263HS, 400245SJ
Known GenesDMD
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)esv3573749
Frequency
Sample Size873
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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