U.S. flag

An official website of the United States government

nsv5557442

  • 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: 76 SVs from 20 studies. See in: genome view    
Submitted genomic173,094,620-173,094,671Question Mark
Overlapping variant regions from other studies: 76 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):172,521,623-172,521,674Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5557442Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5173,094,620173,094,671
nsv5557442RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5172,521,623172,521,674

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16978653sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16978653Submitted genomicNC_000005.10:g.173
094620_173094671in
s522
GRCh38 (hg38)NC_000005.10Chr5173,094,620173,094,671
nssv16978653RemappedPerfectNC_000005.9:g.1725
21623_172521674ins
522
GRCh37.p13First PassNC_000005.9Chr5172,521,623172,521,674

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)
nssv16978653<0.00146404
Support Center