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nsv6469680

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:490

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 132 SVs from 38 studies. See in: genome view    
    Submitted genomic55,890,619-55,891,108Question Mark
    Overlapping variant regions from other studies: 135 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):55,658,095-55,658,584Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6469680Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1155,890,61955,891,108
    nsv6469680RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1155,658,09555,658,584

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17992644deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17992644Submitted genomicNC_000011.10:g.558
    90619_55891108del
    GRCh38 (hg38)NC_000011.10Chr1155,890,61955,891,108
    nssv17992644RemappedPerfectNC_000011.9:g.5565
    8095_55658584del
    GRCh37.p13First PassNC_000011.9Chr1155,658,09555,658,584

    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)
    nssv17992644<0.001335206
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