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nsv5679286

  • 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: 108 SVs from 25 studies. See in: genome view    
Submitted genomic95,793,704-95,793,704Question Mark
Overlapping variant regions from other studies: 108 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):95,423,016-95,423,016Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5679286Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr795,793,70495,793,704
nsv5679286RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr795,423,01695,423,016

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17182209alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17182209Submitted genomicNC_000007.14:g.957
93704_95793705ins1
29
GRCh38 (hg38)NC_000007.14Chr795,793,70495,793,704
nssv17182209RemappedPerfectNC_000007.13:g.954
23016_95423017ins1
29
GRCh37.p13First PassNC_000007.13Chr795,423,01695,423,016

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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