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nsv7074941

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:189,912

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 622 SVs from 57 studies. See in: genome view    
    Submitted genomic40,912,497-41,102,408Question Mark
    Overlapping variant regions from other studies: 622 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):41,204,695-41,394,606Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074941Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1540,912,49741,102,408
    nsv7074941RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1541,204,69541,394,606

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18754758inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18754758Submitted genomicNC_000015.10:g.409
    12497_41102408inv
    GRCh38 (hg38)NC_000015.10Chr1540,912,49741,102,408
    nssv18754758RemappedPerfectNC_000015.9:g.4120
    4695_41394606inv
    GRCh37.p13First PassNC_000015.9Chr1541,204,69541,394,606

    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)
    nssv187547584e-061276268
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