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nsv7055659

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:51

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 335 SVs from 35 studies. See in: genome view    
    Submitted genomic50,993,005-50,993,055Question Mark
    Overlapping variant regions from other studies: 335 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):51,220,143-51,220,193Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7055659Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr250,993,00550,993,055
    nsv7055659RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr251,220,14351,220,193

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18768893inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18768893Submitted genomicNC_000002.12:g.509
    93005_50993055inv
    GRCh38 (hg38)NC_000002.12Chr250,993,00550,993,055
    nssv18768893RemappedPerfectNC_000002.11:g.512
    20143_51220193inv
    GRCh37.p13First PassNC_000002.11Chr251,220,14351,220,193

    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)
    nssv18768893<0.001115273018
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