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nsv930495

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:1,164
  • Description:A processed transcript of the FAM103A1 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: 226 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):166,585,499-166,586,662Question Mark
Overlapping variant regions from other studies: 226 SVs from 38 studies. See in: genome view    
Submitted genomic166,998,987-167,000,150Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv930495RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6166,585,499166,586,662
nsv930495Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6166,998,987167,000,150

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1607664deletionSequencingPaired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1607664RemappedPerfectNC_000006.12:g.(16
6585499_?)_(?_1665
86662)del
GRCh38.p12First PassNC_000006.12Chr6166,585,499166,586,662
nssv1607664Submitted genomicNC_000006.11:g.(16
6998987_?)_(?_1670
00150)del1143
GRCh37 (hg19)NC_000006.11Chr6166,998,987167,000,150

Validation Information

Variant Call IDExperiment IDMethodAnalysisResult
nssv16076642PCRManual observationPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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