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nsv5831079

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,250

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 106 SVs from 22 studies. See in: genome view    
Submitted genomic10,764,838-10,770,087Question Mark
Overlapping variant regions from other studies: 106 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):10,904,964-10,910,213Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5831079Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr210,764,83810,770,087
nsv5831079RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr210,904,96410,910,213

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv17484946copy number variationSequencingSequence alignment2

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17484946Submitted genomicGRCh38 (hg38)NC_000002.12Chr210,764,83810,770,087
nssv17484946RemappedPerfectGRCh37.p13First PassNC_000002.11Chr210,904,96410,910,213

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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