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nsv7060607

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,106,294

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5193 SVs from 94 studies. See in: genome view    
    Submitted genomic46,563,922-48,670,215Question Mark
    Overlapping variant regions from other studies: 5226 SVs from 96 studies. See in: genome view    
    Remapped(Score: Good):44,143,885-46,196,586Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060607Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1846,563,92248,670,215
    nsv7060607RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1844,143,88546,196,586

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759303inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759303Submitted genomicNC_000018.10:g.465
    63922_48670215inv
    GRCh38 (hg38)NC_000018.10Chr1846,563,92248,670,215
    nssv18759303RemappedGoodNC_000018.9:g.4414
    3885_46196586inv
    GRCh37.p13First PassNC_000018.9Chr1844,143,88546,196,586

    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)
    nssv187593037e-062275838
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