A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9770580



Internal ID18307950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39285217..39299714hg38UCSC Ensembl
Innerchr4:39286837..39301334hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3814498
hg1914498
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3569385
Supporting Variants
Samples400833BB
Known GenesMIR1273H, RFC1, WDR19
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=11
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9770580
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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