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nsv6555523

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:639

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 107 SVs from 20 studies. See in: genome view    
    Submitted genomic154,212,678-154,213,316Question Mark
    Overlapping variant regions from other studies: 115 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):154,185,154-154,185,792Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6555523Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1154,212,678154,213,316
    nsv6555523RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1154,185,154154,185,792

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18247081inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18247081Submitted genomicNC_000001.11:g.154
    212678_154213316in
    v
    GRCh38 (hg38)NC_000001.11Chr1154,212,678154,213,316
    nssv18247081RemappedPerfectNC_000001.10:g.154
    185154_154185792in
    v
    GRCh37.p13First PassNC_000001.10Chr1154,185,154154,185,792

    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)
    nssv18247081<0.001235568
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