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nsv7044422

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,561

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 127 SVs from 24 studies. See in: genome view    
    Submitted genomic16,607,834-16,614,394Question Mark
    Overlapping variant regions from other studies: 127 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):16,647,459-16,654,019Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044422Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr716,607,83416,614,394
    nsv7044422RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr716,647,45916,654,019

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18781855inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18781855Submitted genomicNC_000007.14:g.166
    07834_16614394inv
    GRCh38 (hg38)NC_000007.14Chr716,607,83416,614,394
    nssv18781855RemappedPerfectNC_000007.13:g.166
    47459_16654019inv
    GRCh37.p13First PassNC_000007.13Chr716,647,45916,654,019

    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)
    nssv187818554e-061276268
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