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nsv7066896

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,321,202

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 11284 SVs from 114 studies. See in: genome view    
    Submitted genomic76,952,577-79,273,778Question Mark
    Overlapping variant regions from other studies: 11262 SVs from 114 studies. See in: genome view    
    Remapped(Score: Good):74,664,533-77,033,778Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066896Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1876,952,57779,273,778
    nsv7066896RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1874,664,53377,033,778

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759599inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759599Submitted genomicNC_000018.10:g.769
    52577_79273778inv
    GRCh38 (hg38)NC_000018.10Chr1876,952,57779,273,778
    nssv18759599RemappedGoodNC_000018.9:g.7466
    4533_77033778inv
    GRCh37.p13First PassNC_000018.9Chr1874,664,53377,033,778

    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)
    nssv187595994e-061276268
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