A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3578759



Internal ID18360271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34365164..34381734hg38UCSC Ensembl
Innerchr10:34654092..34670662hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3816571
hg1916571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9792981, essv9792979, essv9792980, essv9792976
Samples401691HA, 401016IT, 401281BP, 401749DJ
Known GenesPARD3
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)esv3578759
Frequency
Sample Size873
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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