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nsv6587833

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,021,831

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8795 SVs from 124 studies. See in: genome view    
    Submitted genomic15,680,260-18,702,090Question Mark
    Overlapping variant regions from other studies: 8795 SVs from 124 studies. See in: genome view    
    Remapped(Score: Perfect):15,583,574-18,605,403Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6587833Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1715,680,26018,702,090
    nsv6587833RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1715,583,57418,605,403

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18241396inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18241396Submitted genomicNC_000017.11:g.156
    80260_18702090inv
    GRCh38 (hg38)NC_000017.11Chr1715,680,26018,702,090
    nssv18241396RemappedPerfectNC_000017.10:g.155
    83574_18605403inv
    GRCh37.p13First PassNC_000017.10Chr1715,583,57418,605,403

    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)
    nssv18241396<0.001720354
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