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nsv5892654

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:465,939

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1231 SVs from 78 studies. See in: genome view    
Submitted genomic67,316,665-67,782,603Question Mark
Overlapping variant regions from other studies: 1231 SVs from 78 studies. See in: genome view    
Remapped(Score: Perfect):67,367,089-67,833,027Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5892654Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr367,316,66567,782,603
nsv5892654RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr367,367,08967,833,027

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17410567deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17410567Submitted genomicNC_000003.12:g.673
16665_67782603del
GRCh38 (hg38)NC_000003.12Chr367,316,66567,782,603
nssv17410567RemappedPerfectNC_000003.11:g.673
67089_67833027del
GRCh37.p13First PassNC_000003.11Chr367,367,08967,833,027

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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