U.S. flag

An official website of the United States government

nsv7065788

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,475

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 156 SVs from 25 studies. See in: genome view    
    Submitted genomic97,394,350-97,399,824Question Mark
    Overlapping variant regions from other studies: 156 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):97,937,580-97,943,054Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7065788Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1597,394,35097,399,824
    nsv7065788RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1597,937,58097,943,054

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756729inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756729Submitted genomicNC_000015.10:g.973
    94350_97399824inv
    GRCh38 (hg38)NC_000015.10Chr1597,394,35097,399,824
    nssv18756729RemappedPerfectNC_000015.9:g.9793
    7580_97943054inv
    GRCh37.p13First PassNC_000015.9Chr1597,937,58097,943,054

    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)
    nssv187567291.4e-054276136
    Support Center