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nsv5704158

  • Variant Calls:2
  • 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: 217 SVs from 23 studies. See in: genome view    
Submitted genomic45,522,667-45,522,667Question Mark
Overlapping variant regions from other studies: 217 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):45,918,547-45,918,547Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5704158Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2245,522,66745,522,667
nsv5704158RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2245,918,54745,918,547

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17202183alu insertionSequencingOther
nssv17232339alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17202183Submitted genomicNC_000022.11:g.455
22667_45522668ins2
74
GRCh38 (hg38)NC_000022.11Chr2245,522,66745,522,667
nssv17232339Submitted genomicNC_000022.11:g.455
22667_45522668ins2
80
GRCh38 (hg38)NC_000022.11Chr2245,522,66745,522,667
nssv17202183RemappedPerfectNC_000022.10:g.459
18547_45918548ins2
74
GRCh37.p13First PassNC_000022.10Chr2245,918,54745,918,547
nssv17232339RemappedPerfectNC_000022.10:g.459
18547_45918548ins2
80
GRCh37.p13First PassNC_000022.10Chr2245,918,54745,918,547

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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