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nsv5975179

  • 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: 106 SVs from 16 studies. See in: genome view    
Submitted genomic29,446,434-29,446,434Question Mark
Overlapping variant regions from other studies: 106 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):30,020,571-30,020,571Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5975179Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1329,446,43429,446,434
nsv5975179RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1330,020,57130,020,571

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17385406insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17385406Submitted genomicNC_000013.11:g.294
46434_29446435ins1
76
GRCh38 (hg38)NC_000013.11Chr1329,446,43429,446,434
nssv17385406RemappedPerfectNC_000013.10:g.300
20571_30020572ins1
76
GRCh37.p13First PassNC_000013.10Chr1330,020,57130,020,571

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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