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nsv6579420

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,962,532

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8585 SVs from 124 studies. See in: genome view    
    Submitted genomic15,711,972-18,674,503Question Mark
    Overlapping variant regions from other studies: 8585 SVs from 124 studies. See in: genome view    
    Remapped(Score: Perfect):15,615,286-18,577,816Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6579420Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1715,711,97218,674,503
    nsv6579420RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1715,615,28618,577,816

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18241398inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18241398Submitted genomicNC_000017.11:g.157
    11972_18674503inv
    GRCh38 (hg38)NC_000017.11Chr1715,711,97218,674,503
    nssv18241398RemappedPerfectNC_000017.10:g.156
    15286_18577816inv
    GRCh37.p13First PassNC_000017.10Chr1715,615,28618,577,816

    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)
    nssv18241398<0.001139304
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