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nsv7039147

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:116

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 143 SVs from 20 studies. See in: genome view    
    Submitted genomic20,707,271-20,707,386Question Mark
    Overlapping variant regions from other studies: 143 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):20,708,894-20,709,009Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039147Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr420,707,27120,707,386
    nsv7039147RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr420,708,89420,709,009

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18773363inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18773363Submitted genomicNC_000004.12:g.207
    07271_20707386inv
    GRCh38 (hg38)NC_000004.12Chr420,707,27120,707,386
    nssv18773363RemappedPerfectNC_000004.11:g.207
    08894_20709009inv
    GRCh37.p13First PassNC_000004.11Chr420,708,89420,709,009

    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)
    nssv187733630.0184991273690
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