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nsv4326333

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 20 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):56,893,223-56,893,223Question Mark
Overlapping variant regions from other studies: 19 SVs from 6 studies. See in: genome view    
Submitted genomic54,970,584-54,970,584Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4326333RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1756,893,22356,893,223
nsv4326333Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1754,970,58454,970,584

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16018647insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16018647RemappedPerfectNC_000017.11:g.568
93223_56893224ins2
76
GRCh38.p12First PassNC_000017.11Chr1756,893,22356,893,223
nssv16018647Submitted genomicNC_000017.10:g.549
70584_54970585ins2
76
GRCh37.p13NC_000017.10Chr1754,970,58454,970,584

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)
nssv160186470.01329021686
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