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nsv5650629

  • 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: 101 SVs from 18 studies. See in: genome view    
Submitted genomic40,024,228-40,024,228Question Mark
Overlapping variant regions from other studies: 101 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):40,316,429-40,316,429Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5650629Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1540,024,22840,024,228
nsv5650629RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1540,316,42940,316,429

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17095989insertionHG03125SequencingSequence alignment5,031

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17095989Submitted genomicNC_000015.10:g.400
24228_40024229ins3
23
GRCh38 (hg38)NC_000015.10Chr1540,024,22840,024,228
nssv17095989RemappedPerfectNC_000015.9:g.4031
6429_40316430ins32
3
GRCh37.p13First PassNC_000015.9Chr1540,316,42940,316,429

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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