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nsv5533554

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,034

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 159 SVs from 36 studies. See in: genome view    
Submitted genomic46,789,380-46,802,413Question Mark
Overlapping variant regions from other studies: 159 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):46,823,292-46,836,325Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5533554Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1646,789,38046,802,413
nsv5533554RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1646,823,29246,836,325

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17709338duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17709338Submitted genomicNC_000016.10:g.467
89380_46802413dup
GRCh38 (hg38)NC_000016.10Chr1646,789,38046,802,413
nssv17709338RemappedPerfectNC_000016.9:g.4682
3292_46836325dup
GRCh37.p13First PassNC_000016.9Chr1646,823,29246,836,325

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)
nssv17709338<0.00136404
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