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nsv7062514

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:593

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 140 SVs from 26 studies. See in: genome view    
    Submitted genomic45,123,278-45,123,870Question Mark
    Overlapping variant regions from other studies: 140 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):45,697,413-45,698,005Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7062514Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1345,123,27845,123,870
    nsv7062514RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1345,697,41345,698,005

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18753246inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18753246Submitted genomicNC_000013.11:g.451
    23278_45123870inv
    GRCh38 (hg38)NC_000013.11Chr1345,123,27845,123,870
    nssv18753246RemappedPerfectNC_000013.10:g.456
    97413_45698005inv
    GRCh37.p13First PassNC_000013.10Chr1345,697,41345,698,005

    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)
    nssv18753246<0.001125271850
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