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nsv5692681

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Description:Insertion of a Alu mobile element relative to the reference
  • Publication(s):Chuang et al. 2021

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 143 SVs from 24 studies. See in: genome view    
Submitted genomic89,605,003-89,605,003Question Mark
Overlapping variant regions from other studies: 143 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):90,314,722-90,314,722Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5692681Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr689,605,00389,605,003
nsv5692681RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr690,314,72290,314,722

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17180020alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17180020Submitted genomicNC_000006.12:g.896
05003_89605004ins2
79
GRCh38 (hg38)NC_000006.12Chr689,605,00389,605,003
nssv17180020RemappedPerfectNC_000006.11:g.903
14722_90314723ins2
79
GRCh37.p13First PassNC_000006.11Chr690,314,72290,314,722

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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