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nsv4279578

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,291

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 31 SVs from 8 studies. See in: genome view    
Remapped(Score: Perfect):46,107,765-46,125,055Question Mark
Overlapping variant regions from other studies: 31 SVs from 8 studies. See in: genome view    
Submitted genomic44,736,404-44,753,694Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4279578RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2046,107,76546,125,055
nsv4279578Submitted genomicGRCh37.p13Primary AssemblyNC_000020.10Chr2044,736,40444,753,694

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15964368duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15964368RemappedPerfectNC_000020.11:g.461
07765_46125055dup
GRCh38.p12First PassNC_000020.11Chr2046,107,76546,125,055
nssv15964368Submitted genomicNC_000020.10:g.447
36404_44753694dup
GRCh37.p13NC_000020.10Chr2044,736,40444,753,694

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)
nssv159643684.6e-005121694
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