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nsv5205183

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,058

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 271 SVs from 43 studies. See in: genome view    
Submitted genomic629,026-632,083Question Mark
Overlapping variant regions from other studies: 277 SVs from 44 studies. See in: genome view    
Remapped(Score: Perfect):564,406-567,463Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5205183Submitted genomicGRCh38.p13Primary AssemblyNC_000001.11Chr1629,026632,083
nsv5205183RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1564,406567,463

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16789401copy number variationSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16789401Submitted genomicGRCh38.p13NC_000001.11Chr1629,026632,083
nssv16789401RemappedPerfectGRCh37.p13First PassNC_000001.10Chr1564,406567,463

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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