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nsv7066132

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,720,727

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 17366 SVs from 120 studies. See in: genome view    
    Submitted genomic65,153,239-72,873,965Question Mark
    Overlapping variant regions from other studies: 17366 SVs from 120 studies. See in: genome view    
    Remapped(Score: Perfect):65,547,019-73,267,745Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066132Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1265,153,23972,873,965
    nsv7066132RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1265,547,01973,267,745

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18752732inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18752732Submitted genomicNC_000012.12:g.651
    53239_72873965inv
    GRCh38 (hg38)NC_000012.12Chr1265,153,23972,873,965
    nssv18752732RemappedPerfectNC_000012.11:g.655
    47019_73267745inv
    GRCh37.p13First PassNC_000012.11Chr1265,547,01973,267,745

    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)
    nssv187527321.1e-053270662
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