U.S. flag

An official website of the United States government

nsv5420795

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 106 SVs from 22 studies. See in: genome view    
Submitted genomic51,689,165-51,689,216Question Mark
Overlapping variant regions from other studies: 106 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):51,981,362-51,981,413Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5420795Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1551,689,16551,689,216
nsv5420795RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1551,981,36251,981,413

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17702707alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17702707Submitted genomicNC_000015.10:g.516
89165_51689216ins2
79
GRCh38 (hg38)NC_000015.10Chr1551,689,16551,689,216
nssv17702707RemappedPerfectNC_000015.9:g.5198
1362_51981413ins27
9
GRCh37.p13First PassNC_000015.9Chr1551,981,36251,981,413

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17702707<0.00166404
Support Center