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nsv5243774

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,700

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 484 SVs from 63 studies. See in: genome view    
Submitted genomic6,994,801-6,998,500Question Mark
Overlapping variant regions from other studies: 484 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):6,852,323-6,856,022Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5243774Submitted genomicGRCh38.p13Primary AssemblyNC_000008.11Chr86,994,8016,998,500
nsv5243774RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr86,852,3236,856,022

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16862121copy number variationSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16862121Submitted genomicGRCh38.p13NC_000008.11Chr86,994,8016,998,500
nssv16862121RemappedPerfectGRCh37.p13First PassNC_000008.10Chr86,852,3236,856,022

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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