U.S. flag

An official website of the United States government

nsv5427372

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 83 SVs from 22 studies. See in: genome view    
Submitted genomic24,922,148-24,922,162Question Mark
Overlapping variant regions from other studies: 83 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):24,933,469-24,933,483Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5427372Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1624,922,14824,922,162
nsv5427372RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1624,933,46924,933,483

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17706591alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17706591Submitted genomicNC_000016.10:g.249
22148_24922162ins2
81
GRCh38 (hg38)NC_000016.10Chr1624,922,14824,922,162
nssv17706591RemappedPerfectNC_000016.9:g.2493
3469_24933483ins28
1
GRCh37.p13First PassNC_000016.9Chr1624,933,46924,933,483

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)
nssv17706591<0.00116404
Support Center