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nsv7073594

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,733

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 120 SVs from 28 studies. See in: genome view    
    Submitted genomic40,888,437-40,898,169Question Mark
    Overlapping variant regions from other studies: 120 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):41,180,635-41,190,367Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073594Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1540,888,43740,898,169
    nsv7073594RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1541,180,63541,190,367

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18754757inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18754757Submitted genomicNC_000015.10:g.408
    88437_40898169inv
    GRCh38 (hg38)NC_000015.10Chr1540,888,43740,898,169
    nssv18754757RemappedPerfectNC_000015.9:g.4118
    0635_41190367inv
    GRCh37.p13First PassNC_000015.9Chr1541,180,63541,190,367

    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)
    nssv18754757<0.00165275314
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