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nsv5516818

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:81

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 135 SVs from 20 studies. See in: genome view    
Submitted genomic50,589,895-50,589,975Question Mark
Overlapping variant regions from other studies: 134 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):48,667,256-48,667,336Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5516818Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1750,589,89550,589,975
nsv5516818RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1748,667,25648,667,336

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17724718duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17724718Submitted genomicNC_000017.11:g.505
89895_50589975dup
GRCh38 (hg38)NC_000017.11Chr1750,589,89550,589,975
nssv17724718RemappedPerfectNC_000017.10:g.486
67256_48667336dup
GRCh37.p13First PassNC_000017.10Chr1748,667,25648,667,336

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)
nssv17724718<0.00116404
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