A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1966e212



Internal ID20150422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140448199..140469540hg38UCSC Ensembl
chr7:140147999..140169340hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3821342
hg1921342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3572170, esv3572172, esv3572171
Samples401582GG, 400995MS, 400733SW, 400594VJ, 401263HS
Known GenesMKRN1
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)dgv1966e212
Frequency
Sample Size873
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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