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nsv7059585

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:44

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 70 SVs from 13 studies. See in: genome view    
    Submitted genomic35,451,886-35,451,929Question Mark
    Overlapping variant regions from other studies: 70 SVs from 13 studies. See in: genome view    
    Remapped(Score: Perfect):35,740,814-35,740,857Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059585Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1035,451,88635,451,929
    nsv7059585RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1035,740,81435,740,857

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18749613inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18749613Submitted genomicNC_000010.11:g.354
    51886_35451929inv
    GRCh38 (hg38)NC_000010.11Chr1035,451,88635,451,929
    nssv18749613RemappedPerfectNC_000010.10:g.357
    40814_35740857inv
    GRCh37.p13First PassNC_000010.10Chr1035,740,81435,740,857

    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)
    nssv18749613<0.001171274004
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