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nsv7073384

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:522,559

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1487 SVs from 69 studies. See in: genome view    
    Submitted genomic63,496,011-64,018,569Question Mark
    Overlapping variant regions from other studies: 1488 SVs from 69 studies. See in: genome view    
    Remapped(Score: Perfect):61,163,244-61,685,803Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073384Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1863,496,01164,018,569
    nsv7073384RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1861,163,24461,685,803

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759898inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759898Submitted genomicNC_000018.10:g.634
    96011_64018569inv
    GRCh38 (hg38)NC_000018.10Chr1863,496,01164,018,569
    nssv18759898RemappedPerfectNC_000018.9:g.6116
    3244_61685803inv
    GRCh37.p13First PassNC_000018.9Chr1861,163,24461,685,803

    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)
    nssv187598981.1e-053276258
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