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nsv7050815

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:990,178

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2869 SVs from 93 studies. See in: genome view    
    Submitted genomic240,664,933-241,655,110Question Mark
    Overlapping variant regions from other studies: 2872 SVs from 93 studies. See in: genome view    
    Remapped(Score: Perfect):240,828,233-241,818,412Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7050815Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1240,664,933241,655,110
    nsv7050815RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1240,828,233241,818,412

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759409inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759409Submitted genomicNC_000001.11:g.240
    664933_241655110in
    v
    GRCh38 (hg38)NC_000001.11Chr1240,664,933241,655,110
    nssv18759409RemappedPerfectNC_000001.10:g.240
    828233_241818412in
    v
    GRCh37.p13First PassNC_000001.10Chr1240,828,233241,818,412

    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)
    nssv187594094.6e-0513276198
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