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nsv7040307

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:708,904

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1451 SVs from 74 studies. See in: genome view    
    Submitted genomic73,728,944-74,437,847Question Mark
    Overlapping variant regions from other studies: 1451 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):73,778,095-74,486,998Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7040307Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr373,728,94474,437,847
    nsv7040307RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr373,778,09574,486,998

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18772076inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18772076Submitted genomicNC_000003.12:g.737
    28944_74437847inv
    GRCh38 (hg38)NC_000003.12Chr373,728,94474,437,847
    nssv18772076RemappedPerfectNC_000003.11:g.737
    78095_74486998inv
    GRCh37.p13First PassNC_000003.11Chr373,778,09574,486,998

    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)
    nssv187720761.1e-053275930
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