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nsv7068811

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:54,937

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 424 SVs from 56 studies. See in: genome view    
    Submitted genomic56,133,294-56,188,230Question Mark
    Overlapping variant regions from other studies: 424 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):56,644,663-56,699,599Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7068811Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1956,133,29456,188,230
    nsv7068811RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1956,644,66356,699,599

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761360inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761360Submitted genomicNC_000019.10:g.561
    33294_56188230inv
    GRCh38 (hg38)NC_000019.10Chr1956,133,29456,188,230
    nssv18761360RemappedPerfectNC_000019.9:g.5664
    4663_56699599inv
    GRCh37.p13First PassNC_000019.9Chr1956,644,66356,699,599

    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)
    nssv187613604e-061276268
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