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nsv930470

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:580
  • Description:A processed transcript of the RPL21 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: 202 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):9,156,342-9,156,921Question Mark
Overlapping variant regions from other studies: 202 SVs from 39 studies. See in: genome view    
Submitted genomic9,250,199-9,250,778Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv930470RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr169,156,3429,156,921
nsv930470Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000016.9Chr169,250,1999,250,778

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1607671deletionSequencingPaired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1607671RemappedPerfectNC_000016.10:g.(91
56342_?)_(?_915692
1)del
GRCh38.p12First PassNC_000016.10Chr169,156,3429,156,921
nssv1607671Submitted genomicNC_000016.9:g.(925
0199_?)_(?_9250778
)del512
GRCh37 (hg19)NC_000016.9Chr169,250,1999,250,778

Validation Information

Variant Call IDExperiment IDMethodAnalysisResult
nssv16076712PCRManual observationPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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