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nsv7050840

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:373,982

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1193 SVs from 81 studies. See in: genome view    
    Submitted genomic167,446,684-167,820,665Question Mark
    Overlapping variant regions from other studies: 1078 SVs from 81 studies. See in: genome view    
    Remapped(Score: Good):167,858,901-168,221,345Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7050840Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6167,446,684167,820,665
    nsv7050840RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6167,858,901168,221,345

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18776665inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18776665Submitted genomicNC_000006.12:g.167
    446684_167820665in
    v
    GRCh38 (hg38)NC_000006.12Chr6167,446,684167,820,665
    nssv18776665RemappedGoodNC_000006.11:g.167
    858901_168221345in
    v
    GRCh37.p13First PassNC_000006.11Chr6167,858,901168,221,345

    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)
    nssv187766654e-061276268
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