U.S. flag

An official website of the United States government

nsv6973994

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,202

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 106 SVs from 24 studies. See in: genome view    
    Submitted genomic44,462,086-44,463,287Question Mark
    Overlapping variant regions from other studies: 106 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):44,754,284-44,755,485Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6973994Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1544,462,08644,463,287
    nsv6973994RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1544,754,28444,755,485

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18394710deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18394710Submitted genomicNC_000015.10:g.444
    62086_44463287del
    GRCh38 (hg38)NC_000015.10Chr1544,462,08644,463,287
    nssv18394710RemappedPerfectNC_000015.9:g.4475
    4284_44755485del
    GRCh37.p13First PassNC_000015.9Chr1544,754,28444,755,485

    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)
    nssv183947101.1e-053266902
    Support Center