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nsv7077968

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:274,309

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1093 SVs from 71 studies. See in: genome view    
    Submitted genomic14,024,678-14,298,986Question Mark
    Overlapping variant regions from other studies: 1093 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):14,135,490-14,409,798Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077968Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1914,024,67814,298,986
    nsv7077968RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1914,135,49014,409,798

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18757854inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18757854Submitted genomicNC_000019.10:g.140
    24678_14298986inv
    GRCh38 (hg38)NC_000019.10Chr1914,024,67814,298,986
    nssv18757854RemappedPerfectNC_000019.9:g.1413
    5490_14409798inv
    GRCh37.p13First PassNC_000019.9Chr1914,135,49014,409,798

    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)
    nssv187578544e-061276268
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