A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv709e212



Internal ID20149165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22581937..23102646hg38UCSC Ensembl
chr15:22770422..23291159hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38520710
hg19520738
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3569254, esv3569209, esv3569232, esv3569220, esv3569243
Samples401308LD, 400413FJ, 401386WA, 401230NL, 401259LS
Known GenesCYFIP1, GOLGA8I, HERC2P2, LOC283683, NIPA1, NIPA2, TUBGCP5, WHAMMP3
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)dgv709e212
Frequency
Sample Size873
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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