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nsv5721309

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Description:Insertion of a L1 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: 173 SVs from 26 studies. See in: genome view    
Submitted genomic231,221,240-231,221,240Question Mark
Overlapping variant regions from other studies: 178 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):231,356,986-231,356,986Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5721309Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1231,221,240231,221,240
nsv5721309RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1231,356,986231,356,986

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17244789line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17244789Submitted genomicNC_000001.11:g.231
221240_231221241in
s431
GRCh38 (hg38)NC_000001.11Chr1231,221,240231,221,240
nssv17244789RemappedPerfectNC_000001.10:g.231
356986_231356987in
s431
GRCh37.p13First PassNC_000001.10Chr1231,356,986231,356,986

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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