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nsv5876121

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:781

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 177 SVs from 30 studies. See in: genome view    
Submitted genomic230,272,967-230,273,747Question Mark
Overlapping variant regions from other studies: 182 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):230,408,713-230,409,493Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5876121Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1230,272,967230,273,747
nsv5876121RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1230,408,713230,409,493

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17351493deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17351493Submitted genomicNC_000001.11:g.230
272967_230273747de
l
GRCh38 (hg38)NC_000001.11Chr1230,272,967230,273,747
nssv17351493RemappedPerfectNC_000001.10:g.230
408713_230409493de
l
GRCh37.p13First PassNC_000001.10Chr1230,408,713230,409,493

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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