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nsv6996180

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:324,919

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1317 SVs from 72 studies. See in: genome view    
    Submitted genomic84,119,416-84,444,334Question Mark
    Overlapping variant regions from other studies: 1317 SVs from 72 studies. See in: genome view    
    Remapped(Score: Perfect):84,153,021-84,477,940Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6996180Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1684,119,41684,444,334
    nsv6996180RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1684,153,02184,477,940

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18403689deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18403689Submitted genomicNC_000016.10:g.841
    19416_84444334del
    GRCh38 (hg38)NC_000016.10Chr1684,119,41684,444,334
    nssv18403689RemappedPerfectNC_000016.9:g.8415
    3021_84477940del
    GRCh37.p13First PassNC_000016.9Chr1684,153,02184,477,940

    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)
    nssv184036894e-061276034
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