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nsv4091782

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:70,188

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 65 SVs from 13 studies. See in: genome view    
Remapped(Score: Perfect):49,749,234-49,819,421Question Mark
Overlapping variant regions from other studies: 65 SVs from 13 studies. See in: genome view    
Submitted genomic49,786,667-49,856,854Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4091782RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr349,749,23449,819,421
nsv4091782Submitted genomicGRCh37.p13Primary AssemblyNC_000003.11Chr349,786,66749,856,854

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15972410duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15972410RemappedPerfectNC_000003.12:g.497
49234_49819421dup
GRCh38.p12First PassNC_000003.12Chr349,749,23449,819,421
nssv15972410Submitted genomicNC_000003.11:g.497
86667_49856854dup
GRCh37.p13NC_000003.11Chr349,786,66749,856,854

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)
nssv15972410<0.001521694
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