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nsv7072230

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,585,822

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8849 SVs from 120 studies. See in: genome view    
    Submitted genomic82,484,343-86,070,164Question Mark
    Overlapping variant regions from other studies: 8868 SVs from 120 studies. See in: genome view    
    Remapped(Score: Good):83,396,578-87,082,393Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072230Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr882,484,34386,070,164
    nsv7072230RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr883,396,57887,082,393

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18785402inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18785402Submitted genomicNC_000008.11:g.824
    84343_86070164inv
    GRCh38 (hg38)NC_000008.11Chr882,484,34386,070,164
    nssv18785402RemappedGoodNC_000008.10:g.833
    96578_87082393inv
    GRCh37.p13First PassNC_000008.10Chr883,396,57887,082,393

    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)
    nssv187854024e-061276268
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