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nsv7044173

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,739

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 124 SVs from 23 studies. See in: genome view    
    Submitted genomic16,611,522-16,614,260Question Mark
    Overlapping variant regions from other studies: 124 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):16,651,147-16,653,885Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044173Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr716,611,52216,614,260
    nsv7044173RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr716,651,14716,653,885

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18781856inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18781856Submitted genomicNC_000007.14:g.166
    11522_16614260inv
    GRCh38 (hg38)NC_000007.14Chr716,611,52216,614,260
    nssv18781856RemappedPerfectNC_000007.13:g.166
    51147_16653885inv
    GRCh37.p13First PassNC_000007.13Chr716,651,14716,653,885

    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)
    nssv187818564e-061276268
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