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nsv7043511

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:67

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 108 SVs from 28 studies. See in: genome view    
    Submitted genomic105,224,253-105,224,319Question Mark
    Overlapping variant regions from other studies: 108 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):106,145,410-106,145,476Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7043511Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4105,224,253105,224,319
    nsv7043511RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4106,145,410106,145,476

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18772413inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18772413Submitted genomicNC_000004.12:g.105
    224253_105224319in
    v
    GRCh38 (hg38)NC_000004.12Chr4105,224,253105,224,319
    nssv18772413RemappedPerfectNC_000004.11:g.106
    145410_106145476in
    v
    GRCh37.p13First PassNC_000004.11Chr4106,145,410106,145,476

    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)
    nssv18772413<0.00181273602
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