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nsv5210183

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,700

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 157 SVs from 37 studies. See in: genome view    
Submitted genomic59,843,201-59,853,900Question Mark
Overlapping variant regions from other studies: 157 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):60,308,873-60,319,572Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5210183Submitted genomicGRCh38.p13Primary AssemblyNC_000001.11Chr159,843,20159,853,900
nsv5210183RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr160,308,87360,319,572

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16819901copy number variationSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16819901Submitted genomicGRCh38.p13NC_000001.11Chr159,843,20159,853,900
nssv16819901RemappedPerfectGRCh37.p13First PassNC_000001.10Chr160,308,87360,319,572

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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