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nsv5481845

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:33,273

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 334 SVs from 55 studies. See in: genome view    
Submitted genomic23,163,003-23,196,275Question Mark
Overlapping variant regions from other studies: 334 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):23,020,516-23,053,788Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5481845Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr823,163,00323,196,275
nsv5481845RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr823,020,51623,053,788

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17009871duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17009871Submitted genomicNC_000008.11:g.231
63003_23196275dup
GRCh38 (hg38)NC_000008.11Chr823,163,00323,196,275
nssv17009871RemappedPerfectNC_000008.10:g.230
20516_23053788dup
GRCh37.p13First PassNC_000008.10Chr823,020,51623,053,788

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)
nssv17009871<0.00116404
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