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nsv7077662

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:27,397

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 139 SVs from 32 studies. See in: genome view    
    Submitted genomic61,141,297-61,168,693Question Mark
    Overlapping variant regions from other studies: 139 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):60,908,769-60,936,165Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077662Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1161,141,29761,168,693
    nsv7077662RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1160,908,76960,936,165

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18741633inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18741633Submitted genomicNC_000011.10:g.611
    41297_61168693inv
    GRCh38 (hg38)NC_000011.10Chr1161,141,29761,168,693
    nssv18741633RemappedPerfectNC_000011.9:g.6090
    8769_60936165inv
    GRCh37.p13First PassNC_000011.9Chr1160,908,76960,936,165

    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)
    nssv187416334e-061276268
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