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nsv7075522

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,925,869

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7541 SVs from 106 studies. See in: genome view    
    Submitted genomic38,491,162-41,417,030Question Mark
    Overlapping variant regions from other studies: 7541 SVs from 106 studies. See in: genome view    
    Remapped(Score: Perfect):36,071,126-38,996,994Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7075522Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1838,491,16241,417,030
    nsv7075522RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1836,071,12638,996,994

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759192inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759192Submitted genomicNC_000018.10:g.384
    91162_41417030inv
    GRCh38 (hg38)NC_000018.10Chr1838,491,16241,417,030
    nssv18759192RemappedPerfectNC_000018.9:g.3607
    1126_38996994inv
    GRCh37.p13First PassNC_000018.9Chr1836,071,12638,996,994

    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)
    nssv187591921.1e-053274904
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