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nsv7041415

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:625,235

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1848 SVs from 79 studies. See in: genome view    
    Submitted genomic128,855,871-129,481,105Question Mark
    Overlapping variant regions from other studies: 1848 SVs from 79 studies. See in: genome view    
    Remapped(Score: Perfect):128,574,714-129,199,948Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7041415Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3128,855,871129,481,105
    nsv7041415RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3128,574,714129,199,948

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18769584inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18769584Submitted genomicNC_000003.12:g.128
    855871_129481105in
    v
    GRCh38 (hg38)NC_000003.12Chr3128,855,871129,481,105
    nssv18769584RemappedPerfectNC_000003.11:g.128
    574714_129199948in
    v
    GRCh37.p13First PassNC_000003.11Chr3128,574,714129,199,948

    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)
    nssv187695844e-061276268
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