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nsv5707666

  • 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: 167 SVs from 26 studies. See in: genome view    
Submitted genomic60,412,009-60,412,009Question Mark
Overlapping variant regions from other studies: 167 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):58,489,370-58,489,370Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5707666Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1760,412,00960,412,009
nsv5707666RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1758,489,37058,489,370

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17200373alu insertionSequencingOther
nssv17228510alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17200373Submitted genomicNC_000017.11:g.604
12009_60412010ins1
08
GRCh38 (hg38)NC_000017.11Chr1760,412,00960,412,009
nssv17228510Submitted genomicNC_000017.11:g.604
12009_60412010ins1
08
GRCh38 (hg38)NC_000017.11Chr1760,412,00960,412,009
nssv17200373RemappedPerfectNC_000017.10:g.584
89370_58489371ins1
08
GRCh37.p13First PassNC_000017.10Chr1758,489,37058,489,370
nssv17228510RemappedPerfectNC_000017.10:g.584
89370_58489371ins1
08
GRCh37.p13First PassNC_000017.10Chr1758,489,37058,489,370

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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