A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1371e212



Internal ID22784298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46751582..46808086hg38UCSC Ensembl
chr3:46793072..46849576hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3856505
hg1956505
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3568728, esv3568727, esv3568724, esv3568723, esv3568726, esv3568732, esv3568725
Samples401799DP, 400308SP, 400424LN, 400377WJ, 401380OL, 401962BK, 400683EC, 400655WB, 401845MJ, 400077EB, 400453LN, 400493KH, 401190WC, 401990PR, 401258PC, 402065BG, 400061DE, 400231LP, 400073HT, 400460DM, 401596PJ, 400107MJ, 401979TB, 401785MJ, 400825TW, 400955BE, 400702PA, 401623SN, 401230NL, 401822TL, 401519SA, 401859GS, 401606CG, 400888MS, 400047DS, 400978JG, 400520FM, 400354TJ, 401307VR, 400999HR, 400795CL, 401203MP, 400732MA, 401552BK, 401287CF, 400863SS, 400235MP, 401661HD, 401149VA, 401735LE, 401458RT, 400079AP
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)dgv1371e212
Frequency
Sample Size873
Observed Gain0
Observed Loss52
Observed Complex0
Frequencyn/a


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