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nsv5694428

  • Variant Calls:1
  • 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: 160 SVs from 28 studies. See in: genome view    
Submitted genomic3,112,516-3,112,516Question Mark
Overlapping variant regions from other studies: 160 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):3,162,517-3,162,517Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5694428Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr163,112,5163,112,516
nsv5694428RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr163,162,5173,162,517

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17198277alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17198277Submitted genomicNC_000016.10:g.311
2516_3112517ins281
GRCh38 (hg38)NC_000016.10Chr163,112,5163,112,516
nssv17198277RemappedPerfectNC_000016.9:g.3162
517_3162518ins281
GRCh37.p13First PassNC_000016.9Chr163,162,5173,162,517

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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