A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9826558



Internal ID18311213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:80647670..80755546hg38UCSC Ensembl
InnerchrX:79903169..80011045hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38107877
hg19107877
Variant TypeCNV gain
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3576949
Supporting Variants
Samples400927BD
Known GenesBRWD3
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=252
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9826558
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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