U.S. flag

An official website of the United States government

nsv7065226

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,505,178

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8566 SVs from 113 studies. See in: genome view    
    Submitted genomic98,338,625-100,843,802Question Mark
    Overlapping variant regions from other studies: 8568 SVs from 113 studies. See in: genome view    
    Remapped(Score: Good):98,881,854-101,384,007Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7065226Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1598,338,625100,843,802
    nsv7065226RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1598,881,854101,384,007

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756748inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756748Submitted genomicNC_000015.10:g.983
    38625_100843802inv
    GRCh38 (hg38)NC_000015.10Chr1598,338,625100,843,802
    nssv18756748RemappedGoodNC_000015.9:g.9888
    1854_101384007inv
    GRCh37.p13First PassNC_000015.9Chr1598,881,854101,384,007

    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)
    nssv187567487e-062274720
    Support Center