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nsv7043468

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:307,943

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 707 SVs from 70 studies. See in: genome view    
    Submitted genomic227,499,586-227,807,528Question Mark
    Overlapping variant regions from other studies: 710 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):227,687,287-227,995,229Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7043468Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1227,499,586227,807,528
    nsv7043468RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1227,687,287227,995,229

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761242inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761242Submitted genomicNC_000001.11:g.227
    499586_227807528in
    v
    GRCh38 (hg38)NC_000001.11Chr1227,499,586227,807,528
    nssv18761242RemappedPerfectNC_000001.10:g.227
    687287_227995229in
    v
    GRCh37.p13First PassNC_000001.10Chr1227,687,287227,995,229

    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)
    nssv187612424e-061276268
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