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nsv7059305

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:142

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 126 SVs from 17 studies. See in: genome view    
    Submitted genomic78,105,623-78,105,764Question Mark
    Overlapping variant regions from other studies: 126 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):76,101,704-76,101,845Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059305Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1778,105,62378,105,764
    nsv7059305RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1776,101,70476,101,845

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18757940inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18757940Submitted genomicNC_000017.11:g.781
    05623_78105764inv
    GRCh38 (hg38)NC_000017.11Chr1778,105,62378,105,764
    nssv18757940RemappedPerfectNC_000017.10:g.761
    01704_76101845inv
    GRCh37.p13First PassNC_000017.10Chr1776,101,70476,101,845

    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)
    nssv187579404e-061276248
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