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nsv7076498

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:90,017

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 430 SVs from 44 studies. See in: genome view    
    Submitted genomic49,503,668-49,593,684Question Mark
    Overlapping variant regions from other studies: 430 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):47,030,038-47,120,054Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7076498Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1849,503,66849,593,684
    nsv7076498RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1847,030,03847,120,054

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759943inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759943Submitted genomicNC_000018.10:g.495
    03668_49593684inv
    GRCh38 (hg38)NC_000018.10Chr1849,503,66849,593,684
    nssv18759943RemappedPerfectNC_000018.9:g.4703
    0038_47120054inv
    GRCh37.p13First PassNC_000018.9Chr1847,030,03847,120,054

    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)
    nssv187599437e-062274722
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