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nsv6952539

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:58,230

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 247 SVs from 34 studies. See in: genome view    
    Submitted genomic51,892,188-51,950,417Question Mark
    Overlapping variant regions from other studies: 247 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):52,466,324-52,524,553Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6952539Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1351,892,18851,950,417
    nsv6952539RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1352,466,32452,524,553

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18378418deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18378418Submitted genomicNC_000013.11:g.518
    92188_51950417del
    GRCh38 (hg38)NC_000013.11Chr1351,892,18851,950,417
    nssv18378418RemappedPerfectNC_000013.10:g.524
    66324_52524553del
    GRCh37.p13First PassNC_000013.10Chr1352,466,32452,524,553

    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)
    nssv183784184e-061276250
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