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nsv6519449

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 159 SVs from 42 studies. See in: genome view    
    Submitted genomic50,053,901-50,054,700Question Mark
    Overlapping variant regions from other studies: 159 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):50,557,158-50,557,957Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6519449Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1950,053,90150,054,700
    nsv6519449RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1950,557,15850,557,957

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18049074deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18049074Submitted genomicNC_000019.10:g.500
    53901_50054700del
    GRCh38 (hg38)NC_000019.10Chr1950,053,90150,054,700
    nssv18049074RemappedPerfectNC_000019.9:g.5055
    7158_50557957del
    GRCh37.p13First PassNC_000019.9Chr1950,557,15850,557,957

    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)
    nssv18049074<0.001135808
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