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nsv5468457

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,811

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 161 SVs from 41 studies. See in: genome view    
Submitted genomic73,129,801-73,132,611Question Mark
Overlapping variant regions from other studies: 161 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):73,995,518-73,998,328Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5468457Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr473,129,80173,132,611
nsv5468457RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr473,995,51873,998,328

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16952226deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16952226Submitted genomicNC_000004.12:g.731
29801_73132611del
GRCh38 (hg38)NC_000004.12Chr473,129,80173,132,611
nssv16952226RemappedPerfectNC_000004.11:g.739
95518_73998328del
GRCh37.p13First PassNC_000004.11Chr473,995,51873,998,328

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)
nssv16952226<0.00136404
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