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nsv7048011

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35,649

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 375 SVs from 71 studies. See in: genome view    
    Submitted genomic16,867,829-16,903,477Question Mark
    Overlapping variant regions from other studies: 375 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):16,907,453-16,943,101Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048011Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr716,867,82916,903,477
    nsv7048011RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr716,907,45316,943,101

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18781859inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18781859Submitted genomicNC_000007.14:g.168
    67829_16903477inv
    GRCh38 (hg38)NC_000007.14Chr716,867,82916,903,477
    nssv18781859RemappedPerfectNC_000007.13:g.169
    07453_16943101inv
    GRCh37.p13First PassNC_000007.13Chr716,907,45316,943,101

    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)
    nssv187818594e-061276268
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