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nsv7066294

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,736

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 126 SVs from 26 studies. See in: genome view    
    Submitted genomic88,210,243-88,213,978Question Mark
    Overlapping variant regions from other studies: 126 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):88,753,474-88,757,209Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066294Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1588,210,24388,213,978
    nsv7066294RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1588,753,47488,757,209

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756085inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756085Submitted genomicNC_000015.10:g.882
    10243_88213978inv
    GRCh38 (hg38)NC_000015.10Chr1588,210,24388,213,978
    nssv18756085RemappedPerfectNC_000015.9:g.8875
    3474_88757209inv
    GRCh37.p13First PassNC_000015.9Chr1588,753,47488,757,209

    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)
    nssv187560854e-061276268
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