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nsv6575523

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,213,284

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 16795 SVs from 113 studies. See in: genome view    
    Submitted genomic72,881,788-80,095,071Question Mark
    Overlapping variant regions from other studies: 16797 SVs from 113 studies. See in: genome view    
    Remapped(Score: Perfect):73,794,023-81,007,306Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6575523Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr872,881,78880,095,071
    nsv6575523RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr873,794,02381,007,306

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18278656inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18278656Submitted genomicNC_000008.11:g.728
    81788_80095071inv
    GRCh38 (hg38)NC_000008.11Chr872,881,78880,095,071
    nssv18278656RemappedPerfectNC_000008.10:g.737
    94023_81007306inv
    GRCh37.p13First PassNC_000008.10Chr873,794,02381,007,306

    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)
    nssv18278656<0.001139304
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