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nsv5259092

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,100

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 472 SVs from 63 studies. See in: genome view    
Submitted genomic6,998,701-6,999,800Question Mark
Overlapping variant regions from other studies: 472 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):6,856,223-6,857,322Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5259092Submitted genomicGRCh38.p13Primary AssemblyNC_000008.11Chr86,998,7016,999,800
nsv5259092RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr86,856,2236,857,322

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16859875copy number variationSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16859875Submitted genomicGRCh38.p13NC_000008.11Chr86,998,7016,999,800
nssv16859875RemappedPerfectGRCh37.p13First PassNC_000008.10Chr86,856,2236,857,322

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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