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nsv7075031

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:608,673

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1746 SVs from 82 studies. See in: genome view    
    Submitted genomic42,968,972-43,577,644Question Mark
    Overlapping variant regions from other studies: 1746 SVs from 82 studies. See in: genome view    
    Remapped(Score: Perfect):41,597,612-42,206,284Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7075031Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2042,968,97243,577,644
    nsv7075031RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2041,597,61242,206,284

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18762036inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18762036Submitted genomicNC_000020.11:g.429
    68972_43577644inv
    GRCh38 (hg38)NC_000020.11Chr2042,968,97243,577,644
    nssv18762036RemappedPerfectNC_000020.10:g.415
    97612_42206284inv
    GRCh37.p13First PassNC_000020.10Chr2041,597,61242,206,284

    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)
    nssv187620364e-061276268
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