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nsv5702732

  • 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: 86 SVs from 19 studies. See in: genome view    
Submitted genomic81,473,182-81,473,182Question Mark
Overlapping variant regions from other studies: 86 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):81,939,526-81,939,526Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5702732Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1481,473,18281,473,182
nsv5702732RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1481,939,52681,939,526

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17196623alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17196623Submitted genomicNC_000014.9:g.8147
3182_81473183ins27
9
GRCh38 (hg38)NC_000014.9Chr1481,473,18281,473,182
nssv17196623RemappedPerfectNC_000014.8:g.8193
9526_81939527ins27
9
GRCh37.p13First PassNC_000014.8Chr1481,939,52681,939,526

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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