U.S. flag

An official website of the United States government

nsv5713081

  • 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: 121 SVs from 23 studies. See in: genome view    
Submitted genomic51,689,165-51,689,165Question Mark
Overlapping variant regions from other studies: 121 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):51,981,362-51,981,362Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5713081Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1551,689,16551,689,165
nsv5713081RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1551,981,36251,981,362

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17197499alu insertionSequencingOther
nssv17227722alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17197499Submitted genomicNC_000015.10:g.516
89165_51689166ins2
79
GRCh38 (hg38)NC_000015.10Chr1551,689,16551,689,165
nssv17227722Submitted genomicNC_000015.10:g.516
89165_51689166ins2
79
GRCh38 (hg38)NC_000015.10Chr1551,689,16551,689,165
nssv17197499RemappedPerfectNC_000015.9:g.5198
1362_51981363ins27
9
GRCh37.p13First PassNC_000015.9Chr1551,981,36251,981,362
nssv17227722RemappedPerfectNC_000015.9:g.5198
1362_51981363ins27
9
GRCh37.p13First PassNC_000015.9Chr1551,981,36251,981,362

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.

Support Center