A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv302e212



Internal ID22783229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126913842..126924681hg38UCSC Ensembl
chr10:128602411..128613250hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3810840
hg1910840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3579221, esv3579220
Samples401102RD, 401799DP, 401749DJ, 400145BL, 401465TB, 400336BG, 401415CB, 401427CB, 401674DD, 401355CD, 400486LS, 401495NR, 401175FA, 401594MP, 401119DK, 400960TN, 401526WB, 400381CA, 401326LI, 400124FR, 400006DK, 400371GA, 401203MP, 401428LD, 401314MK, 400044HS, 401152MV, 400108BJ, 400209BS, 400012CJ
Known GenesDOCK1
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)dgv302e212
Frequency
Sample Size873
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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