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nsv7054458

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:22

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 100 SVs from 17 studies. See in: genome view    
    Submitted genomic111,582,776-111,582,797Question Mark
    Overlapping variant regions from other studies: 100 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):111,903,979-111,904,000Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7054458Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6111,582,776111,582,797
    nsv7054458RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6111,903,979111,904,000

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18777834inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18777834Submitted genomicNC_000006.12:g.111
    582776_111582797in
    v
    GRCh38 (hg38)NC_000006.12Chr6111,582,776111,582,797
    nssv18777834RemappedPerfectNC_000006.11:g.111
    903979_111904000in
    v
    GRCh37.p13First PassNC_000006.11Chr6111,903,979111,904,000

    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)
    nssv187778344e-061276266
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