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nsv5876111

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:80

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 168 SVs from 34 studies. See in: genome view    
Submitted genomic61,969,998-61,970,077Question Mark
Overlapping variant regions from other studies: 168 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):62,435,670-62,435,749Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5876111Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr161,969,99861,970,077
nsv5876111RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr162,435,67062,435,749

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17379492deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17379492Submitted genomicNC_000001.11:g.619
69998_61970077del
GRCh38 (hg38)NC_000001.11Chr161,969,99861,970,077
nssv17379492RemappedPerfectNC_000001.10:g.624
35670_62435749del
GRCh37.p13First PassNC_000001.10Chr162,435,67062,435,749

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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