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nsv6571433

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:482

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 178 SVs from 34 studies. See in: genome view    
    Submitted genomic164,917,316-164,917,797Question Mark
    Overlapping variant regions from other studies: 178 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):165,838,468-165,838,949Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6571433Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4164,917,316164,917,797
    nsv6571433RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4165,838,468165,838,949

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18264911inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18264911Submitted genomicNC_000004.12:g.164
    917316_164917797in
    v
    GRCh38 (hg38)NC_000004.12Chr4164,917,316164,917,797
    nssv18264911RemappedPerfectNC_000004.11:g.165
    838468_165838949in
    v
    GRCh37.p13First PassNC_000004.11Chr4165,838,468165,838,949

    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)
    nssv18264911<0.0012333112
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