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nsv4330625

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,995,156

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2868 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):2,515,505-5,510,660Question Mark
Overlapping variant regions from other studies: 2868 SVs from 22 studies. See in: genome view    
Submitted genomic2,496,151-5,491,306Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4330625RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr202,515,5055,510,660
nsv4330625Submitted genomicGRCh37.p13Primary AssemblyNC_000020.10Chr202,496,1515,491,306

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091261inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091261RemappedPerfectNC_000020.11:g.251
5505_5510660inv
GRCh38.p12First PassNC_000020.11Chr202,515,5055,510,660
nssv16091261Submitted genomicNC_000020.10:g.249
6151_5491306inv
GRCh37.p13NC_000020.10Chr202,496,1515,491,306

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)
nssv160912614.6e-005121694
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