A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv28e212



Internal ID20148484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36412423..36438579hg38UCSC Ensembl
chr1:36878024..36904180hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3826157
hg1926157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3577809, esv3577812, esv3577810, esv3577813, esv3577811
Samples400926LJ, 400534ME, 400739SS, 401146US, 400313DF, 401117NA, 401783BD, 400897MD, 400199SA, 401308LD, 400073HT, 401165SB, 401038LN, 401994BD, 401532LJ, 401801LA, 401717LP, 401419SW, 401892MJ, 400520FM, 401307VR, 401268PS, 402048WB, 4000046CJ, 401166WJ, 400106PC, 400130HA, 400108BJ, 401628GC, 400540BM, 400532MH, 401246HH, 401362ME
Known GenesOSCP1
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)dgv28e212
Frequency
Sample Size873
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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