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nsv930487

  • Variant Calls:1
  • Validation:Fail
  • Clinical Assertions: No
  • Region Size:1,975
  • Description:A processed transcript of the FAM133B 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: 94 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):61,375,058-61,377,032Question Mark
Overlapping variant regions from other studies: 94 SVs from 19 studies. See in: genome view    
Submitted genomic60,670,885-60,672,859Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv930487RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr561,375,05861,377,032
nsv930487Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000005.9Chr560,670,88560,672,859

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1607665deletionSequencingPaired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1607665RemappedPerfectNC_000005.10:g.(61
375058_?)_(?_61377
032)del
GRCh38.p12First PassNC_000005.10Chr561,375,05861,377,032
nssv1607665Submitted genomicNC_000005.9:g.(606
70885_?)_(?_606728
59)del1969
GRCh37 (hg19)NC_000005.9Chr560,670,88560,672,859

Validation Information

Variant Call IDExperiment IDMethodAnalysisResult
nssv16076652PCRManual observationFail

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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