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nsv6106309

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:128,488

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 384 SVs from 57 studies. See in: genome view    
Submitted genomic16,062,087-16,190,574Question Mark
Overlapping variant regions from other studies: 384 SVs from 57 studies. See in: genome view    
Remapped(Score: Perfect):16,103,594-16,232,081Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6106309Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr316,062,08716,190,574
nsv6106309RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr316,103,59416,232,081

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17549467inversionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17549467Submitted genomicNC_000003.12:g.160
62087_16190574inv
GRCh38 (hg38)NC_000003.12Chr316,062,08716,190,574
nssv17549467RemappedPerfectNC_000003.11:g.161
03594_16232081inv
GRCh37.p13First PassNC_000003.11Chr316,103,59416,232,081

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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