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nsv6407453

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,850

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 94 SVs from 21 studies. See in: genome view    
    Submitted genomic139,415,962-139,418,811Question Mark
    Overlapping variant regions from other studies: 94 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):138,751,651-138,754,500Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6407453Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5139,415,962139,418,811
    nsv6407453RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5138,751,651138,754,500

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18125413deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18125413Submitted genomicNC_000005.10:g.139
    415962_139418811de
    l
    GRCh38 (hg38)NC_000005.10Chr5139,415,962139,418,811
    nssv18125413RemappedPerfectNC_000005.9:g.1387
    51651_138754500del
    GRCh37.p13First PassNC_000005.9Chr5138,751,651138,754,500

    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)
    nssv18125413<0.001138992
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