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nsv4087719

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:86,757

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 65 SVs from 12 studies. See in: genome view    
Remapped(Score: Perfect):22,753,237-22,839,993Question Mark
Overlapping variant regions from other studies: 65 SVs from 12 studies. See in: genome view    
Submitted genomic22,794,728-22,881,484Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4087719RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr322,753,23722,839,993
nsv4087719Submitted genomicGRCh37.p13Primary AssemblyNC_000003.11Chr322,794,72822,881,484

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15879348deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15879348RemappedPerfectNC_000003.12:g.227
53237_22839993del
GRCh38.p12First PassNC_000003.12Chr322,753,23722,839,993
nssv15879348Submitted genomicNC_000003.11:g.227
94728_22881484del
GRCh37.p13NC_000003.11Chr322,794,72822,881,484

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)
nssv15879348<0.001921694
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