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nsv5221097

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:61,900

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 309 SVs from 46 studies. See in: genome view    
Submitted genomic42,781,801-42,843,700Question Mark
Overlapping variant regions from other studies: 309 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):42,749,539-42,811,438Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5221097Submitted genomicGRCh38.p13Primary AssemblyNC_000006.12Chr642,781,80142,843,700
nsv5221097RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr642,749,53942,811,438

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16848043copy number variationSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16848043Submitted genomicGRCh38.p13NC_000006.12Chr642,781,80142,843,700
nssv16848043RemappedPerfectGRCh37.p13First PassNC_000006.11Chr642,749,53942,811,438

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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