U.S. flag

An official website of the United States government

nsv5409667

  • 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: 96 SVs from 19 studies. See in: genome view    
Submitted genomic87,215,153-87,215,204Question Mark
Overlapping variant regions from other studies: 96 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):87,924,871-87,924,922Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5409667Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr687,215,15387,215,204
nsv5409667RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr687,924,87187,924,922

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16984972alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16984972Submitted genomicNC_000006.12:g.872
15153_87215204ins2
80
GRCh38 (hg38)NC_000006.12Chr687,215,15387,215,204
nssv16984972RemappedPerfectNC_000006.11:g.879
24871_87924922ins2
80
GRCh37.p13First PassNC_000006.11Chr687,924,87187,924,922

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)
nssv169849720.007446404
Support Center