U.S. flag

An official website of the United States government

nsv7058629

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26,017

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 209 SVs from 48 studies. See in: genome view    
    Submitted genomic57,822,861-57,848,877Question Mark
    Overlapping variant regions from other studies: 209 SVs from 48 studies. See in: genome view    
    Remapped(Score: Perfect):58,334,229-58,360,245Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058629Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1957,822,86157,848,877
    nsv7058629RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1958,334,22958,360,245

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761404inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761404Submitted genomicNC_000019.10:g.578
    22861_57848877inv
    GRCh38 (hg38)NC_000019.10Chr1957,822,86157,848,877
    nssv18761404RemappedPerfectNC_000019.9:g.5833
    4229_58360245inv
    GRCh37.p13First PassNC_000019.9Chr1958,334,22958,360,245

    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)
    nssv187614044e-061276268
    Support Center