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nsv7058586

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,579

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 126 SVs from 33 studies. See in: genome view    
    Submitted genomic87,898,731-87,904,309Question Mark
    Overlapping variant regions from other studies: 126 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):87,609,623-87,615,201Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058586Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1187,898,73187,904,309
    nsv7058586RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1187,609,62387,615,201

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18746716inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18746716Submitted genomicNC_000011.10:g.878
    98731_87904309inv
    GRCh38 (hg38)NC_000011.10Chr1187,898,73187,904,309
    nssv18746716RemappedPerfectNC_000011.9:g.8760
    9623_87615201inv
    GRCh37.p13First PassNC_000011.9Chr1187,609,62387,615,201

    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)
    nssv187467164e-061276268
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