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nsv7074157

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,960,183

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4638 SVs from 95 studies. See in: genome view    
    Submitted genomic51,800,664-53,760,846Question Mark
    Overlapping variant regions from other studies: 4638 SVs from 95 studies. See in: genome view    
    Remapped(Score: Perfect):52,267,382-54,227,564Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074157Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1451,800,66453,760,846
    nsv7074157RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1452,267,38254,227,564

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18754308inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18754308Submitted genomicNC_000014.9:g.5180
    0664_53760846inv
    GRCh38 (hg38)NC_000014.9Chr1451,800,66453,760,846
    nssv18754308RemappedPerfectNC_000014.8:g.5226
    7382_54227564inv
    GRCh37.p13First PassNC_000014.8Chr1452,267,38254,227,564

    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)
    nssv187543087e-062274040
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