A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1036e212



Internal ID20149492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30265044..30283329hg38UCSC Ensembl
chr19:30755951..30774236hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3818286
hg1918286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3583343, esv3583344
Samples401146US, 400132HN, 401029SD, 400768MN, 401618HR, 401326LI, 401711WS, 401259LS, 400156WT, 400267GD, 400328LM
Known Genes
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)dgv1036e212
Frequency
Sample Size873
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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