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nsv930497

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:3,511
  • Description:A processed transcript of the DHFR 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: 252 SVs from 50 studies. See in: genome view    
Remapped(Score: Perfect):26,167,847-26,171,357Question Mark
Overlapping variant regions from other studies: 252 SVs from 50 studies. See in: genome view    
Submitted genomic23,747,811-23,751,321Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv930497RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr1826,167,84726,171,357
nsv930497Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000018.9Chr1823,747,81123,751,321

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1607663deletionSequencingPaired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1607663RemappedPerfectNC_000018.10:g.(26
167847_?)_(?_26171
357)del
GRCh38.p12First PassNC_000018.10Chr1826,167,84726,171,357
nssv1607663Submitted genomicNC_000018.9:g.(237
47811_?)_(?_237513
21)del3494
GRCh37 (hg19)NC_000018.9Chr1823,747,81123,751,321

Validation Information

Variant Call IDExperiment IDMethodAnalysisResult
nssv16076632PCRManual observationPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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