A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1024e212



Internal ID22783951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17178031..17214428hg38UCSC Ensembl
chr19:17288840..17325237hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3836398
hg1936398
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3583268, esv3583267
Samples400002HK, 400818BL, 401517PR
Known GenesMYO9B
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)dgv1024e212
Frequency
Sample Size873
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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