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nsv930485

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:465
  • Description:A processed transcript of the RPS26 gene was reverse transcribed and reinserted into the genome. Since the insertion was detected in the reference assembly but not in a test sample, by convention it must be referred to here as a deletion.
  • Publication(s):Schrider et al. 2013

Genome View

Select assembly:
Overlapping variant regions from other studies: 178 SVs from 54 studies. See in: genome view    
Remapped(Score: Perfect):113,213,956-113,214,420Question Mark
Overlapping variant regions from other studies: 178 SVs from 54 studies. See in: genome view    
Submitted genomic114,135,112-114,135,576Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv930485RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr4113,213,956113,214,420
nsv930485Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000004.11Chr4114,135,112114,135,576

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1607676deletionSequencingPaired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1607676RemappedPerfectNC_000004.12:g.(11
3213956_?)_(?_1132
14420)del
GRCh38.p12First PassNC_000004.12Chr4113,213,956113,214,420
nssv1607676Submitted genomicNC_000004.11:g.(11
4135112_?)_(?_1141
35576)del442
GRCh37 (hg19)NC_000004.11Chr4114,135,112114,135,576

Validation Information

Variant Call IDExperiment IDMethodAnalysisResult
nssv16076762PCRManual observationPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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