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nsv7063845

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,541,454

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3655 SVs from 96 studies. See in: genome view    
    Submitted genomic82,252,671-83,794,124Question Mark
    Overlapping variant regions from other studies: 3808 SVs from 98 studies. See in: genome view    
    Remapped(Score: Pass):82,545,012-84,462,876Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7063845Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1582,252,67183,794,124
    nsv7063845RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1582,545,01284,462,876

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755168inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755168Submitted genomicNC_000015.10:g.822
    52671_83794124inv
    GRCh38 (hg38)NC_000015.10Chr1582,252,67183,794,124
    nssv18755168RemappedPassNC_000015.9:g.8254
    5012_84462876inv
    GRCh37.p13First PassNC_000015.9Chr1582,545,01284,462,876

    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)
    nssv187551687e-062276254
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