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nsv930483

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:331
  • Description:A processed transcript of the RPL36A 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: 138 SVs from 54 studies. See in: genome view    
Remapped(Score: Perfect):16,974,714-16,975,044Question Mark
Overlapping variant regions from other studies: 138 SVs from 54 studies. See in: genome view    
Submitted genomic16,996,261-16,996,591Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv930483RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1116,974,71416,975,044
nsv930483Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1116,996,26116,996,591

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1607674deletionSequencingPaired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1607674RemappedPerfectNC_000011.10:g.(16
974714_?)_(?_16975
044)del
GRCh38.p12First PassNC_000011.10Chr1116,974,71416,975,044
nssv1607674Submitted genomicNC_000011.9:g.(169
96261_?)_(?_169965
91)del398
GRCh37 (hg19)NC_000011.9Chr1116,996,26116,996,591

Validation Information

Variant Call IDExperiment IDMethodAnalysisResult
nssv16076742PCRManual observationPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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