U.S. flag

An official website of the United States government

nsv7062907

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:935,660

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2937 SVs from 117 studies. See in: genome view    
    Submitted genomic21,501,792-22,437,451Question Mark
    Overlapping variant regions from other studies: 2937 SVs from 117 studies. See in: genome view    
    Remapped(Score: Perfect):21,513,113-22,448,772Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7062907Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1621,501,79222,437,451
    nsv7062907RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1621,513,11322,448,772

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756419inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756419Submitted genomicNC_000016.10:g.215
    01792_22437451inv
    GRCh38 (hg38)NC_000016.10Chr1621,501,79222,437,451
    nssv18756419RemappedPerfectNC_000016.9:g.2151
    3113_22448772inv
    GRCh37.p13First PassNC_000016.9Chr1621,513,11322,448,772

    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)
    nssv187564190.04210682255604
    Support Center