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nsv5706345

  • 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: 214 SVs from 21 studies. See in: genome view    
Submitted genomic45,531,227-45,531,227Question Mark
Overlapping variant regions from other studies: 214 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):45,927,107-45,927,107Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5706345Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2245,531,22745,531,227
nsv5706345RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2245,927,10745,927,107

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17202185alu insertionSequencingOther
nssv17223806alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17202185Submitted genomicNC_000022.11:g.455
31227_45531228ins2
81
GRCh38 (hg38)NC_000022.11Chr2245,531,22745,531,227
nssv17223806Submitted genomicNC_000022.11:g.455
31227_45531228ins2
81
GRCh38 (hg38)NC_000022.11Chr2245,531,22745,531,227
nssv17202185RemappedPerfectNC_000022.10:g.459
27107_45927108ins2
81
GRCh37.p13First PassNC_000022.10Chr2245,927,10745,927,107
nssv17223806RemappedPerfectNC_000022.10:g.459
27107_45927108ins2
81
GRCh37.p13First PassNC_000022.10Chr2245,927,10745,927,107

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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