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nsv6978019

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:49,770

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 206 SVs from 53 studies. See in: genome view    
    Submitted genomic85,885,660-85,935,429Question Mark
    Overlapping variant regions from other studies: 206 SVs from 53 studies. See in: genome view    
    Remapped(Score: Perfect):86,352,004-86,401,773Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6978019Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1485,885,66085,935,429
    nsv6978019RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1486,352,00486,401,773

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18391490deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18391490Submitted genomicNC_000014.9:g.8588
    5660_85935429del
    GRCh38 (hg38)NC_000014.9Chr1485,885,66085,935,429
    nssv18391490RemappedPerfectNC_000014.8:g.8635
    2004_86401773del
    GRCh37.p13First PassNC_000014.8Chr1486,352,00486,401,773

    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)
    nssv183914904e-061273990
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