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nsv5298973

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:260,700

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1229 SVs from 74 studies. See in: genome view    
Submitted genomic74,951,501-75,212,200Question Mark
Overlapping variant regions from other studies: 1229 SVs from 74 studies. See in: genome view    
Remapped(Score: Perfect):72,947,596-73,208,295Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5298973Submitted genomicGRCh38.p13Primary AssemblyNC_000017.11Chr1774,951,50175,212,200
nsv5298973RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1772,947,59673,208,295

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16825374copy number variationSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16825374Submitted genomicGRCh38.p13NC_000017.11Chr1774,951,50175,212,200
nssv16825374RemappedPerfectGRCh37.p13First PassNC_000017.10Chr1772,947,59673,208,295

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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