A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv141e212



Internal ID20148597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207534320..207575509hg38UCSC Ensembl
chr1:207707665..207748854hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3841190
hg1941190
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3575460, esv3575617, esv3575595, esv3575472, esv3575628, esv3575606
Samples401808PS, 401386WA, 400663MD, 401432SB, 401311GL, 401087SF, 400295PS, 401735LE, 401102RD
Known GenesCR1
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)dgv141e212
Frequency
Sample Size873
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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