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nsv5521879

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:915

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 93 SVs from 24 studies. See in: genome view    
Submitted genomic50,503,109-50,504,023Question Mark
Overlapping variant regions from other studies: 93 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):51,006,366-51,007,280Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5521879Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1950,503,10950,504,023
nsv5521879RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1951,006,36651,007,280

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17725306duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17725306Submitted genomicNC_000019.10:g.505
03109_50504023dup
GRCh38 (hg38)NC_000019.10Chr1950,503,10950,504,023
nssv17725306RemappedPerfectNC_000019.9:g.5100
6366_51007280dup
GRCh37.p13First PassNC_000019.9Chr1951,006,36651,007,280

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)
nssv17725306<0.00126404
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