A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1888e212



Internal ID20150344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38246914..38355256hg38UCSC Ensembl
chr7:38286515..38394857hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38108343
hg19108343
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3576321, esv3576313, esv3576312, esv3576320, esv3576334, esv3576322, esv3576315, esv3576337, esv3576310, esv3576318, esv3576330, esv3576329, esv3576325, esv3576333, esv3576314
Samples400911GA, 401400NP, 400554WB, 401734PG, 400294HD, 400622SJ, 401096SL, 400298ME, 400588BE, 400817MB, 400113LD, 400107MJ, 401234MB, 401377MA, 401729AC, 401262RR, 401844ZD, 400508RD, 401612HB, 401993HM, 401068SD, 400982BS
Known GenesTARP, TRG-AS1
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)dgv1888e212
Frequency
Sample Size873
Observed Gain22
Observed Loss0
Observed Complex0
Frequencyn/a


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