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nsv5707223

  • 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: 142 SVs from 30 studies. See in: genome view    
Submitted genomic62,406,066-62,406,066Question Mark
Overlapping variant regions from other studies: 142 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):60,483,427-60,483,427Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5707223Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1762,406,06662,406,066
nsv5707223RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1760,483,42760,483,427

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17198438alu insertionSequencingOther
nssv17233320alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17198438Submitted genomicNC_000017.11:g.624
06066_62406067ins2
81
GRCh38 (hg38)NC_000017.11Chr1762,406,06662,406,066
nssv17233320Submitted genomicNC_000017.11:g.624
06066_62406067ins2
81
GRCh38 (hg38)NC_000017.11Chr1762,406,06662,406,066
nssv17198438RemappedPerfectNC_000017.10:g.604
83427_60483428ins2
81
GRCh37.p13First PassNC_000017.10Chr1760,483,42760,483,427
nssv17233320RemappedPerfectNC_000017.10:g.604
83427_60483428ins2
81
GRCh37.p13First PassNC_000017.10Chr1760,483,42760,483,427

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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