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nsv5475960

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,324

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 198 SVs from 35 studies. See in: genome view    
Submitted genomic43,065,188-43,066,511Question Mark
Overlapping variant regions from other studies: 198 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):42,920,331-42,921,654Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5475960Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr843,065,18843,066,511
nsv5475960RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr842,920,33142,921,654

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17009845deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17009845Submitted genomicNC_000008.11:g.430
65188_43066511del
GRCh38 (hg38)NC_000008.11Chr843,065,18843,066,511
nssv17009845RemappedPerfectNC_000008.10:g.429
20331_42921654del
GRCh37.p13First PassNC_000008.10Chr842,920,33142,921,654

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)
nssv170098450.0231506404
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