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nsv7075020

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:74,371

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 349 SVs from 47 studies. See in: genome view    
    Submitted genomic73,579,650-73,654,020Question Mark
    Overlapping variant regions from other studies: 349 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):73,613,549-73,687,919Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7075020Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1673,579,65073,654,020
    nsv7075020RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1673,613,54973,687,919

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758258inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758258Submitted genomicNC_000016.10:g.735
    79650_73654020inv
    GRCh38 (hg38)NC_000016.10Chr1673,579,65073,654,020
    nssv18758258RemappedPerfectNC_000016.9:g.7361
    3549_73687919inv
    GRCh37.p13First PassNC_000016.9Chr1673,613,54973,687,919

    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)
    nssv187582580.012785272020
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