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nsv5935589

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:22,700

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 277 SVs from 41 studies. See in: genome view    
Submitted genomic75,866,413-75,889,112Question Mark
Overlapping variant regions from other studies: 277 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):73,862,494-73,885,193Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5935589Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1775,866,41375,889,112
nsv5935589RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1773,862,49473,885,193

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17379029deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17379029Submitted genomicNC_000017.11:g.758
66413_75889112del
GRCh38 (hg38)NC_000017.11Chr1775,866,41375,889,112
nssv17379029RemappedPerfectNC_000017.10:g.738
62494_73885193del
GRCh37.p13First PassNC_000017.10Chr1773,862,49473,885,193

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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