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nsv7068275

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,156

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 80 SVs from 27 studies. See in: genome view    
    Submitted genomic124,258,169-124,260,324Question Mark
    Overlapping variant regions from other studies: 80 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):127,020,448-127,022,603Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7068275Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9124,258,169124,260,324
    nsv7068275RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9127,020,448127,022,603

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18784353inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18784353Submitted genomicNC_000009.12:g.124
    258169_124260324in
    v
    GRCh38 (hg38)NC_000009.12Chr9124,258,169124,260,324
    nssv18784353RemappedPerfectNC_000009.11:g.127
    020448_127022603in
    v
    GRCh37.p13First PassNC_000009.11Chr9127,020,448127,022,603

    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)
    nssv187843531.1e-053274030
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