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nsv5407149

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 95 SVs from 24 studies. See in: genome view    
Submitted genomic46,226,202-46,226,253Question Mark
Overlapping variant regions from other studies: 95 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):46,267,693-46,267,744Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5407149Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr346,226,20246,226,253
nsv5407149RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr346,267,69346,267,744

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16933291alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16933291Submitted genomicNC_000003.12:g.462
26202_46226253ins2
81
GRCh38 (hg38)NC_000003.12Chr346,226,20246,226,253
nssv16933291RemappedPerfectNC_000003.11:g.462
67693_46267744ins2
81
GRCh37.p13First PassNC_000003.11Chr346,267,69346,267,744

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)
nssv16933291<0.00116404
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