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nsv7058867

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:437,807

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1635 SVs from 88 studies. See in: genome view    
    Submitted genomic86,821,907-87,259,713Question Mark
    Overlapping variant regions from other studies: 1635 SVs from 88 studies. See in: genome view    
    Remapped(Score: Perfect):88,581,664-89,019,470Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058867Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1086,821,90787,259,713
    nsv7058867RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1088,581,66489,019,470

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18740428inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18740428Submitted genomicNC_000010.11:g.868
    21907_87259713inv
    GRCh38 (hg38)NC_000010.11Chr1086,821,90787,259,713
    nssv18740428RemappedPerfectNC_000010.10:g.885
    81664_89019470inv
    GRCh37.p13First PassNC_000010.10Chr1088,581,66489,019,470

    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)
    nssv187404283.9e-0511273470
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