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nsv4505219

  • 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: 17 SVs from 3 studies. See in: genome view    
Remapped(Score: Perfect):46,127,003-46,127,003Question Mark
Overlapping variant regions from other studies: 17 SVs from 3 studies. See in: genome view    
Submitted genomic44,755,642-44,755,642Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4505219RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2046,127,00346,127,003
nsv4505219Submitted genomicGRCh37.p13Primary AssemblyNC_000020.10Chr2044,755,64244,755,642

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16033097alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16033097RemappedPerfectNC_000020.11:g.461
27003_46127004ins2
81
GRCh38.p12First PassNC_000020.11Chr2046,127,00346,127,003
nssv16033097Submitted genomicNC_000020.10:g.447
55642_44755643ins2
81
GRCh37.p13NC_000020.10Chr2044,755,64244,755,642

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)
nssv160330974.6e-005121694
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