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nsv7065801

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,704,940

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6139 SVs from 104 studies. See in: genome view    
    Submitted genomic2,987,267-4,692,206Question Mark
    Overlapping variant regions from other studies: 6139 SVs from 104 studies. See in: genome view    
    Remapped(Score: Perfect):3,029,459-4,734,398Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7065801Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr102,987,2674,692,206
    nsv7065801RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr103,029,4594,734,398

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18735514inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18735514Submitted genomicNC_000010.11:g.298
    7267_4692206inv
    GRCh38 (hg38)NC_000010.11Chr102,987,2674,692,206
    nssv18735514RemappedPerfectNC_000010.10:g.302
    9459_4734398inv
    GRCh37.p13First PassNC_000010.10Chr103,029,4594,734,398

    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)
    nssv187355144e-061276266
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