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nsv7038109

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,737,037

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 18710 SVs from 125 studies. See in: genome view    
    Submitted genomic125,606,921-134,343,957Question Mark
    Overlapping variant regions from other studies: 18710 SVs from 125 studies. See in: genome view    
    Remapped(Score: Perfect):125,928,067-134,665,095Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7038109Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6125,606,921134,343,957
    nsv7038109RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6125,928,067134,665,095

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18779443inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18779443Submitted genomicNC_000006.12:g.125
    606921_134343957in
    v
    GRCh38 (hg38)NC_000006.12Chr6125,606,921134,343,957
    nssv18779443RemappedPerfectNC_000006.11:g.125
    928067_134665095in
    v
    GRCh37.p13First PassNC_000006.11Chr6125,928,067134,665,095

    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)
    nssv187794430.0225875271716
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