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nsv5213581

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26,193

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 279 SVs from 56 studies. See in: genome view    
Submitted genomic109,618,275-109,644,467Question Mark
Overlapping variant regions from other studies: 281 SVs from 56 studies. See in: genome view    
Remapped(Score: Perfect):110,160,897-110,187,089Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5213581Submitted genomicGRCh38.p13Primary AssemblyNC_000001.11Chr1109,618,275109,644,467
nsv5213581RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1110,160,897110,187,089

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16785770copy number variationSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16785770Submitted genomicGRCh38.p13NC_000001.11Chr1109,618,275109,644,467
nssv16785770RemappedPerfectGRCh37.p13First PassNC_000001.10Chr1110,160,897110,187,089

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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