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nsv7050407

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,017,669

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4420 SVs from 110 studies. See in: genome view    
    Submitted genomic5,896,320-6,913,988Question Mark
    Overlapping variant regions from other studies: 4420 SVs from 110 studies. See in: genome view    
    Remapped(Score: Perfect):5,935,951-6,953,619Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7050407Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr75,896,3206,913,988
    nsv7050407RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr75,935,9516,953,619

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18780723inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18780723Submitted genomicNC_000007.14:g.589
    6320_6913988inv
    GRCh38 (hg38)NC_000007.14Chr75,896,3206,913,988
    nssv18780723RemappedPerfectNC_000007.13:g.593
    5951_6953619inv
    GRCh37.p13First PassNC_000007.13Chr75,935,9516,953,619

    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)
    nssv187807234e-061276268
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