U.S. flag

An official website of the United States government

nsv5298869

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,718

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 218 SVs from 42 studies. See in: genome view    
Submitted genomic11,928,633-11,933,350Question Mark
Overlapping variant regions from other studies: 218 SVs from 42 studies. See in: genome view    
Remapped(Score: Perfect):11,988,690-11,993,407Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5298869Submitted genomicGRCh38.p13Primary AssemblyNC_000001.11Chr111,928,63311,933,350 (-1)
nsv5298869RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr111,988,69011,993,407 (-1)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16748520deletionSequencingSplit read and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16748520Submitted genomicNC_000001.11:g.119
28633_(11933349_?)
del
GRCh38.p13NC_000001.11Chr111,928,63311,933,350 (-1)
nssv16748520RemappedPerfectNC_000001.10:g.119
88690_(11993406_?)
del
GRCh37.p13First PassNC_000001.10Chr111,988,69011,993,407 (-1)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)
nssv167485200.031
Support Center