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nsv7055145

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,522

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 142 SVs from 31 studies. See in: genome view    
    Submitted genomic122,954,436-122,956,957Question Mark
    Overlapping variant regions from other studies: 142 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):123,875,591-123,878,112Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7055145Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4122,954,436122,956,957
    nsv7055145RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4123,875,591123,878,112

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18772846inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18772846Submitted genomicNC_000004.12:g.122
    954436_122956957in
    v
    GRCh38 (hg38)NC_000004.12Chr4122,954,436122,956,957
    nssv18772846RemappedPerfectNC_000004.11:g.123
    875591_123878112in
    v
    GRCh37.p13First PassNC_000004.11Chr4123,875,591123,878,112

    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)
    nssv187728464e-061276268
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