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nsv5886621

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,400

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 300 SVs from 30 studies. See in: genome view    
Submitted genomic99,390,616-99,392,015Question Mark
Overlapping variant regions from other studies: 300 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):99,930,821-99,932,220Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5886621Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1599,390,61699,392,015
nsv5886621RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1599,930,82199,932,220

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv17475047copy number variationSequencingSequence alignment2

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17475047Submitted genomicGRCh38 (hg38)NC_000015.10Chr1599,390,61699,392,015
nssv17475047RemappedPerfectGRCh37.p13First PassNC_000015.9Chr1599,930,82199,932,220

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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