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nsv930482

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:491
  • Description:A processed transcript of the RPL3 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

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 85 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):98,972,811-98,973,301Question Mark
Overlapping variant regions from other studies: 85 SVs from 18 studies. See in: genome view    
Submitted genomic99,439,148-99,439,638Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv930482RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1498,972,81198,973,301
nsv930482Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000014.8Chr1499,439,14899,439,638

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1607673deletionSequencingPaired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1607673RemappedPerfectNC_000014.9:g.(989
72811_?)_(?_989733
01)del
GRCh38.p12First PassNC_000014.9Chr1498,972,81198,973,301
nssv1607673Submitted genomicNC_000014.8:g.(994
39148_?)_(?_994396
38)del478
GRCh37 (hg19)NC_000014.8Chr1499,439,14899,439,638

Validation Information

Variant Call IDExperiment IDMethodAnalysisResult
nssv16076732PCRManual observationPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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