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nsv7047105

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,127

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 131 SVs from 21 studies. See in: genome view    
    Submitted genomic144,001,853-144,008,979Question Mark
    Overlapping variant regions from other studies: 131 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):144,759,420-144,766,546Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7047105Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2144,001,853144,008,979
    nsv7047105RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2144,759,420144,766,546

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765887inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765887Submitted genomicNC_000002.12:g.144
    001853_144008979in
    v
    GRCh38 (hg38)NC_000002.12Chr2144,001,853144,008,979
    nssv18765887RemappedPerfectNC_000002.11:g.144
    759420_144766546in
    v
    GRCh37.p13First PassNC_000002.11Chr2144,759,420144,766,546

    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)
    nssv187658874e-061276268
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