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nsv7011134

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,479

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 331 SVs from 40 studies. See in: genome view    
    Submitted genomic1,473,815-1,480,293Question Mark
    Overlapping variant regions from other studies: 331 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):1,473,814-1,480,292Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7011134Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr191,473,8151,480,293
    nsv7011134RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr191,473,8141,480,292

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18422393deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18422393Submitted genomicNC_000019.10:g.147
    3815_1480293del
    GRCh38 (hg38)NC_000019.10Chr191,473,8151,480,293
    nssv18422393RemappedPerfectNC_000019.9:g.1473
    814_1480292del
    GRCh37.p13First PassNC_000019.9Chr191,473,8141,480,292

    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)
    nssv184223931.4e-054276222
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