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nsv5674690

  • 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: 114 SVs from 26 studies. See in: genome view    
Submitted genomic22,211,123-22,211,123Question Mark
Overlapping variant regions from other studies: 114 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):22,250,742-22,250,742Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5674690Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr722,211,12322,211,123
nsv5674690RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr722,250,74222,250,742

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17181626alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17181626Submitted genomicNC_000007.14:g.222
11123_22211124ins2
80
GRCh38 (hg38)NC_000007.14Chr722,211,12322,211,123
nssv17181626RemappedPerfectNC_000007.13:g.222
50742_22250743ins2
80
GRCh37.p13First PassNC_000007.13Chr722,250,74222,250,742

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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