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nsv930496

  • Variant Calls:1
  • Validation:Fail
  • Clinical Assertions: No
  • Region Size:1,183
  • Description:A processed transcript of the SDHC 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: 258 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):1,857,279-1,858,461Question Mark
Overlapping variant regions from other studies: 258 SVs from 34 studies. See in: genome view    
Submitted genomic1,760,573-1,761,755Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv930496RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr171,857,2791,858,461
nsv930496Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000017.10Chr171,760,5731,761,755

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1607677deletionSequencingPaired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1607677RemappedPerfectNC_000017.11:g.(18
57279_?)_(?_185846
1)del
GRCh38.p12First PassNC_000017.11Chr171,857,2791,858,461
nssv1607677Submitted genomicNC_000017.10:g.(17
60573_?)_(?_176175
5)del1182
GRCh37 (hg19)NC_000017.10Chr171,760,5731,761,755

Validation Information

Variant Call IDExperiment IDMethodAnalysisResult
nssv16076772PCRManual observationFail

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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