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nsv930468

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:1,135
  • Description:A processed transcript of the GCSH 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: 192 SVs from 52 studies. See in: genome view    
Remapped(Score: Perfect):168,055,359-168,056,493Question Mark
Overlapping variant regions from other studies: 195 SVs from 52 studies. See in: genome view    
Submitted genomic168,024,597-168,025,731Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv930468RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1168,055,359168,056,493
nsv930468Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1168,024,597168,025,731

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1607666deletionSequencingPaired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1607666RemappedPerfectNC_000001.11:g.(16
8055359_?)_(?_1680
56493)del
GRCh38.p12First PassNC_000001.11Chr1168,055,359168,056,493
nssv1607666Submitted genomicNC_000001.10:g.(16
8024597_?)_(?_1680
25731)del1134
GRCh37 (hg19)NC_000001.10Chr1168,024,597168,025,731

Validation Information

Variant Call IDExperiment IDMethodAnalysisResult
nssv16076662PCRManual observationPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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