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nsv5722942

  • 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: 485 SVs from 39 studies. See in: genome view    
Submitted genomic6,560,903-6,560,903Question Mark
Overlapping variant regions from other studies: 488 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):6,560,903-6,560,903Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5722942Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr96,560,9036,560,903
nsv5722942RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr96,560,9036,560,903

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17239027line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17239027Submitted genomicNC_000009.12:g.656
0903_6560904ins70
GRCh38 (hg38)NC_000009.12Chr96,560,9036,560,903
nssv17239027RemappedPerfectNC_000009.11:g.656
0903_6560904ins70
GRCh37.p13First PassNC_000009.11Chr96,560,9036,560,903

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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