U.S. flag

An official website of the United States government

nsv5411431

  • 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: 180 SVs from 36 studies. See in: genome view    
Submitted genomic131,594,661-131,594,712Question Mark
Overlapping variant regions from other studies: 180 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):132,352,234-132,352,285Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5411431Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2131,594,661131,594,712
nsv5411431RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2132,352,234132,352,285

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16917843alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16917843Submitted genomicNC_000002.12:g.131
594661_131594712in
s264
GRCh38 (hg38)NC_000002.12Chr2131,594,661131,594,712
nssv16917843RemappedPerfectNC_000002.11:g.132
352234_132352285in
s264
GRCh37.p13First PassNC_000002.11Chr2132,352,234132,352,285

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)
nssv16917843<0.00126404
Support Center