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nsv7044040

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:226,202

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 693 SVs from 77 studies. See in: genome view    
    Submitted genomic149,831,135-150,057,336Question Mark
    Overlapping variant regions from other studies: 693 SVs from 77 studies. See in: genome view    
    Remapped(Score: Perfect):150,152,271-150,378,472Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044040Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6149,831,135150,057,336
    nsv7044040RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6150,152,271150,378,472

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18779082inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18779082Submitted genomicNC_000006.12:g.149
    831135_150057336in
    v
    GRCh38 (hg38)NC_000006.12Chr6149,831,135150,057,336
    nssv18779082RemappedPerfectNC_000006.11:g.150
    152271_150378472in
    v
    GRCh37.p13First PassNC_000006.11Chr6150,152,271150,378,472

    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)
    nssv187790821.4e-054274684
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