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nsv7068424

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,278,856

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3010 SVs from 77 studies. See in: genome view    
    Submitted genomic75,621,086-76,899,941Question Mark
    Overlapping variant regions from other studies: 3010 SVs from 77 studies. See in: genome view    
    Remapped(Score: Perfect):76,014,866-77,293,721Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7068424Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1275,621,08676,899,941
    nsv7068424RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1276,014,86677,293,721

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18753460inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18753460Submitted genomicNC_000012.12:g.756
    21086_76899941inv
    GRCh38 (hg38)NC_000012.12Chr1275,621,08676,899,941
    nssv18753460RemappedPerfectNC_000012.11:g.760
    14866_77293721inv
    GRCh37.p13First PassNC_000012.11Chr1276,014,86677,293,721

    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)
    nssv187534604e-061276268
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