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nsv7048604

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,882

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 105 SVs from 23 studies. See in: genome view    
    Submitted genomic73,812,646-73,816,527Question Mark
    Overlapping variant regions from other studies: 105 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):73,861,797-73,865,678Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048604Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr373,812,64673,816,527
    nsv7048604RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr373,861,79773,865,678

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18772078inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18772078Submitted genomicNC_000003.12:g.738
    12646_73816527inv
    GRCh38 (hg38)NC_000003.12Chr373,812,64673,816,527
    nssv18772078RemappedPerfectNC_000003.11:g.738
    61797_73865678inv
    GRCh37.p13First PassNC_000003.11Chr373,861,79773,865,678

    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)
    nssv187720784e-061276268
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