U.S. flag

An official website of the United States government

nsv5407415

  • 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: 137 SVs from 19 studies. See in: genome view    
Submitted genomic182,381,542-182,381,593Question Mark
Overlapping variant regions from other studies: 139 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):182,350,677-182,350,728Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5407415Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1182,381,542182,381,593
nsv5407415RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1182,350,677182,350,728

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16892787alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16892787Submitted genomicNC_000001.11:g.182
381542_182381593in
s269
GRCh38 (hg38)NC_000001.11Chr1182,381,542182,381,593
nssv16892787RemappedPerfectNC_000001.10:g.182
350677_182350728in
s269
GRCh37.p13First PassNC_000001.10Chr1182,350,677182,350,728

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)
nssv16892787<0.00136404
Support Center