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nsv5294162

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:488,000

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2157 SVs from 84 studies. See in: genome view    
Submitted genomic3,332,801-3,820,800Question Mark
Overlapping variant regions from other studies: 2157 SVs from 84 studies. See in: genome view    
Remapped(Score: Perfect):3,332,799-3,820,798Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5294162Submitted genomicGRCh38.p13Primary AssemblyNC_000019.10Chr193,332,8013,820,800
nsv5294162RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr193,332,7993,820,798

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16826712copy number variationSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16826712Submitted genomicGRCh38.p13NC_000019.10Chr193,332,8013,820,800
nssv16826712RemappedPerfectGRCh37.p13First PassNC_000019.9Chr193,332,7993,820,798

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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