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nsv6720857

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 90 SVs from 26 studies. See in: genome view    
    Submitted genomic55,487,273-55,490,372Question Mark
    Overlapping variant regions from other studies: 90 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):56,353,440-56,356,539Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6720857Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr455,487,27355,490,372
    nsv6720857RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr456,353,44056,356,539

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18497238deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18497238Submitted genomicNC_000004.12:g.554
    87273_55490372del
    GRCh38 (hg38)NC_000004.12Chr455,487,27355,490,372
    nssv18497238RemappedPerfectNC_000004.11:g.563
    53440_56356539del
    GRCh37.p13First PassNC_000004.11Chr456,353,44056,356,539

    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)
    nssv184972381.4e-054275870
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