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nsv7066862

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,052,629

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8895 SVs from 124 studies. See in: genome view    
    Submitted genomic15,664,455-18,717,083Question Mark
    Overlapping variant regions from other studies: 8895 SVs from 124 studies. See in: genome view    
    Remapped(Score: Perfect):15,567,769-18,620,396Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066862Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1715,664,45518,717,083
    nsv7066862RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1715,567,76918,620,396

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756157inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756157Submitted genomicNC_000017.11:g.156
    64455_18717083inv
    GRCh38 (hg38)NC_000017.11Chr1715,664,45518,717,083
    nssv18756157RemappedPerfectNC_000017.10:g.155
    67769_18620396inv
    GRCh37.p13First PassNC_000017.10Chr1715,567,76918,620,396

    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)
    nssv187561574.7e-0513270234
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