U.S. flag

An official website of the United States government

nsv5408160

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 80 SVs from 18 studies. See in: genome view    
Submitted genomic86,969,773-86,969,790Question Mark
Overlapping variant regions from other studies: 80 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):87,018,923-87,018,940Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5408160Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr386,969,77386,969,790
nsv5408160RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr387,018,92387,018,940

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16936661alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16936661Submitted genomicNC_000003.12:g.869
69773_86969790ins2
81
GRCh38 (hg38)NC_000003.12Chr386,969,77386,969,790
nssv16936661RemappedPerfectNC_000003.11:g.870
18923_87018940ins2
81
GRCh37.p13First PassNC_000003.11Chr387,018,92387,018,940

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)
nssv16936661<0.00116404
Support Center