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nsv5722168

  • Variant Calls:2
  • 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: 135 SVs from 27 studies. See in: genome view    
Submitted genomic44,270,801-44,270,801Question Mark
Overlapping variant regions from other studies: 135 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):44,736,473-44,736,473Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5722168Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr144,270,80144,270,801
nsv5722168RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr144,736,47344,736,473

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17239732line1 insertionSequencingOther
nssv17248312line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17239732Submitted genomicNC_000001.11:g.442
70801_44270802ins5
64
GRCh38 (hg38)NC_000001.11Chr144,270,80144,270,801
nssv17248312Submitted genomicNC_000001.11:g.442
70801_44270802ins5
64
GRCh38 (hg38)NC_000001.11Chr144,270,80144,270,801
nssv17239732RemappedPerfectNC_000001.10:g.447
36473_44736474ins5
64
GRCh37.p13First PassNC_000001.10Chr144,736,47344,736,473
nssv17248312RemappedPerfectNC_000001.10:g.447
36473_44736474ins5
64
GRCh37.p13First PassNC_000001.10Chr144,736,47344,736,473

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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