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nsv5240251

  • 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: 179 SVs from 34 studies. See in: genome view    
Submitted genomic112,846,001-112,849,700Question Mark
Overlapping variant regions from other studies: 179 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):112,564,848-112,568,547Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5240251Submitted genomicGRCh38.p13Primary AssemblyNC_000003.12Chr3112,846,001112,849,700
nsv5240251RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3112,564,848112,568,547

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16849216copy number variationSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16849216Submitted genomicGRCh38.p13NC_000003.12Chr3112,846,001112,849,700
nssv16849216RemappedPerfectGRCh37.p13First PassNC_000003.11Chr3112,564,848112,568,547

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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