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nsv7077782

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,122

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 78 SVs from 18 studies. See in: genome view    
    Submitted genomic78,804,635-78,807,756Question Mark
    Overlapping variant regions from other studies: 78 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):79,270,978-79,274,099Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077782Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1478,804,63578,807,756
    nsv7077782RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1479,270,97879,274,099

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18754646inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18754646Submitted genomicNC_000014.9:g.7880
    4635_78807756inv
    GRCh38 (hg38)NC_000014.9Chr1478,804,63578,807,756
    nssv18754646RemappedPerfectNC_000014.8:g.7927
    0978_79274099inv
    GRCh37.p13First PassNC_000014.8Chr1479,270,97879,274,099

    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)
    nssv187546464e-061276266
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