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nsv6543196

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:674

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 110 SVs from 20 studies. See in: genome view    
    Submitted genomic117,007,521-117,008,194Question Mark
    Overlapping variant regions from other studies: 112 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):117,550,143-117,550,816Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6543196Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1117,007,521117,008,194
    nsv6543196RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1117,550,143117,550,816

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18249864inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18249864Submitted genomicNC_000001.11:g.117
    007521_117008194in
    v
    GRCh38 (hg38)NC_000001.11Chr1117,007,521117,008,194
    nssv18249864RemappedPerfectNC_000001.10:g.117
    550143_117550816in
    v
    GRCh37.p13First PassNC_000001.10Chr1117,550,143117,550,816

    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)
    nssv18249864<0.001134122
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