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nsv6565866

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:676

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 21 studies. See in: genome view    
    Submitted genomic89,847,285-89,847,960Question Mark
    Overlapping variant regions from other studies: 104 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):90,557,004-90,557,679Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6565866Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr689,847,28589,847,960
    nsv6565866RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr690,557,00490,557,679

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18272121inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18272121Submitted genomicNC_000006.12:g.898
    47285_89847960inv
    GRCh38 (hg38)NC_000006.12Chr689,847,28589,847,960
    nssv18272121RemappedPerfectNC_000006.11:g.905
    57004_90557679inv
    GRCh37.p13First PassNC_000006.11Chr690,557,00490,557,679

    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)
    nssv18272121<0.0011134226
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