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nsv7072404

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:248,038

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1349 SVs from 80 studies. See in: genome view    
    Submitted genomic8,651,745-8,899,782Question Mark
    Overlapping variant regions from other studies: 1349 SVs from 80 studies. See in: genome view    
    Remapped(Score: Perfect):8,745,602-8,993,639Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072404Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr168,651,7458,899,782
    nsv7072404RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr168,745,6028,993,639

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18757089inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18757089Submitted genomicNC_000016.10:g.865
    1745_8899782inv
    GRCh38 (hg38)NC_000016.10Chr168,651,7458,899,782
    nssv18757089RemappedPerfectNC_000016.9:g.8745
    602_8993639inv
    GRCh37.p13First PassNC_000016.9Chr168,745,6028,993,639

    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)
    nssv187570894e-061276268
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