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nsv6507845

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:628,549

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1885 SVs from 84 studies. See in: genome view    
    Submitted genomic62,220,975-62,849,523Question Mark
    Overlapping variant regions from other studies: 1885 SVs from 84 studies. See in: genome view    
    Remapped(Score: Perfect):62,513,174-63,141,722Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6507845Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1562,220,97562,849,523
    nsv6507845RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1562,513,17463,141,722

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18185824duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18185824Submitted genomicNC_000015.10:g.622
    20975_62849523dup
    GRCh38 (hg38)NC_000015.10Chr1562,220,97562,849,523
    nssv18185824RemappedPerfectNC_000015.9:g.6251
    3174_63141722dup
    GRCh37.p13First PassNC_000015.9Chr1562,513,17463,141,722

    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)
    nssv18185824<0.001139284
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