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nsv5533419

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:63

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 109 SVs from 19 studies. See in: genome view    
Submitted genomic55,849,309-55,849,371Question Mark
Overlapping variant regions from other studies: 109 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):56,141,507-56,141,569Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5533419Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1555,849,30955,849,371
nsv5533419RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1556,141,50756,141,569

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17699825duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17699825Submitted genomicNC_000015.10:g.558
49309_55849371dup
GRCh38 (hg38)NC_000015.10Chr1555,849,30955,849,371
nssv17699825RemappedPerfectNC_000015.9:g.5614
1507_56141569dup
GRCh37.p13First PassNC_000015.9Chr1556,141,50756,141,569

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17699825<0.00116404
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