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nsv930481

  • Variant Calls:1
  • Validation:Fail
  • Clinical Assertions: No
  • Region Size:655
  • Description:A processed transcript of the RPL29 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: 137 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):117,998,928-117,999,582Question Mark
Overlapping variant regions from other studies: 137 SVs from 23 studies. See in: genome view    
Submitted genomic118,320,091-118,320,745Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv930481RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6117,998,928117,999,582
nsv930481Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6118,320,091118,320,745

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1607672deletionSequencingPaired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1607672RemappedPerfectNC_000006.12:g.(11
7998928_?)_(?_1179
99582)del
GRCh38.p12First PassNC_000006.12Chr6117,998,928117,999,582
nssv1607672Submitted genomicNC_000006.11:g.(11
8320091_?)_(?_1183
20745)del640
GRCh37 (hg19)NC_000006.11Chr6118,320,091118,320,745

Validation Information

Variant Call IDExperiment IDMethodAnalysisResult
nssv16076722PCRManual observationFail

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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