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nsv7060951

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,142,934

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 17140 SVs from 118 studies. See in: genome view    
    Submitted genomic76,824,737-79,967,670Question Mark
    Overlapping variant regions from other studies: 17118 SVs from 118 studies. See in: genome view    
    Remapped(Score: Good):74,536,693-77,727,670Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060951Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1876,824,73779,967,670
    nsv7060951RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1874,536,69377,727,670

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759593inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759593Submitted genomicNC_000018.10:g.768
    24737_79967670inv
    GRCh38 (hg38)NC_000018.10Chr1876,824,73779,967,670
    nssv18759593RemappedGoodNC_000018.9:g.7453
    6693_77727670inv
    GRCh37.p13First PassNC_000018.9Chr1874,536,69377,727,670

    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)
    nssv187595934e-061276268
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