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nsv6562590

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:777

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 91 SVs from 21 studies. See in: genome view    
    Submitted genomic42,195,350-42,196,126Question Mark
    Overlapping variant regions from other studies: 91 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):42,163,088-42,163,864Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6562590Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr642,195,35042,196,126
    nsv6562590RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr642,163,08842,163,864

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18271285inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18271285Submitted genomicNC_000006.12:g.421
    95350_42196126inv
    GRCh38 (hg38)NC_000006.12Chr642,195,35042,196,126
    nssv18271285RemappedPerfectNC_000006.11:g.421
    63088_42163864inv
    GRCh37.p13First PassNC_000006.11Chr642,163,08842,163,864

    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)
    nssv18271285<0.001233854
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