A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9832697



Internal ID18678799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:140722033..140724090hg38UCSC Ensembl
InnerchrX:139804198..139806255hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg382058
hg192058
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3574835
Supporting Variants
Samples401538NS
Known GenesLINC00632
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=36
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9832697
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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