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nsv7067245

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,098,802

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 10645 SVs from 115 studies. See in: genome view    
    Submitted genomic103,215,092-107,313,893Question Mark
    Overlapping variant regions from other studies: 10647 SVs from 115 studies. See in: genome view    
    Remapped(Score: Perfect):103,085,821-107,184,619Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067245Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11103,215,092107,313,893
    nsv7067245RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11103,085,821107,184,619

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18738214inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18738214Submitted genomicNC_000011.10:g.103
    215092_107313893in
    v
    GRCh38 (hg38)NC_000011.10Chr11103,215,092107,313,893
    nssv18738214RemappedPerfectNC_000011.9:g.1030
    85821_107184619inv
    GRCh37.p13First PassNC_000011.9Chr11103,085,821107,184,619

    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)
    nssv187382144e-061276268
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