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nsv7073439

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,184,827

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 9378 SVs from 119 studies. See in: genome view    
    Submitted genomic15,962,151-19,146,977Question Mark
    Overlapping variant regions from other studies: 9378 SVs from 119 studies. See in: genome view    
    Remapped(Score: Perfect):15,865,465-19,050,290Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073439Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1715,962,15119,146,977
    nsv7073439RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1715,865,46519,050,290

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756163inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756163Submitted genomicNC_000017.11:g.159
    62151_19146977inv
    GRCh38 (hg38)NC_000017.11Chr1715,962,15119,146,977
    nssv18756163RemappedPerfectNC_000017.10:g.158
    65465_19050290inv
    GRCh37.p13First PassNC_000017.10Chr1715,865,46519,050,290

    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)
    nssv187561634e-061276268
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