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nsv7055093

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,992

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 196 SVs from 32 studies. See in: genome view    
    Submitted genomic50,628,669-50,633,660Question Mark
    Overlapping variant regions from other studies: 196 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):50,855,807-50,860,798Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7055093Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr250,628,66950,633,660
    nsv7055093RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr250,855,80750,860,798

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18768886inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18768886Submitted genomicNC_000002.12:g.506
    28669_50633660inv
    GRCh38 (hg38)NC_000002.12Chr250,628,66950,633,660
    nssv18768886RemappedPerfectNC_000002.11:g.508
    55807_50860798inv
    GRCh37.p13First PassNC_000002.11Chr250,855,80750,860,798

    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)
    nssv187688864e-061276268
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