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nsv7076046

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,916,807

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7732 SVs from 112 studies. See in: genome view    
    Submitted genomic42,633,367-44,550,173Question Mark
    Overlapping variant regions from other studies: 7516 SVs from 112 studies. See in: genome view    
    Remapped(Score: Good):44,053,477-45,916,560Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7076046Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2142,633,36744,550,173
    nsv7076046RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2144,053,47745,916,560

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18762779inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18762779Submitted genomicNC_000021.9:g.4263
    3367_44550173inv
    GRCh38 (hg38)NC_000021.9Chr2142,633,36744,550,173
    nssv18762779RemappedGoodNC_000021.8:g.4405
    3477_45916560inv
    GRCh37.p13First PassNC_000021.8Chr2144,053,47745,916,560

    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)
    nssv187627794e-061276268
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