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nsv6547038

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:802

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 153 SVs from 21 studies. See in: genome view    
    Submitted genomic224,407,007-224,407,808Question Mark
    Overlapping variant regions from other studies: 156 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):224,594,709-224,595,510Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6547038Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1224,407,007224,407,808
    nsv6547038RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1224,594,709224,595,510

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18249379inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18249379Submitted genomicNC_000001.11:g.224
    407007_224407808in
    v
    GRCh38 (hg38)NC_000001.11Chr1224,407,007224,407,808
    nssv18249379RemappedPerfectNC_000001.10:g.224
    594709_224595510in
    v
    GRCh37.p13First PassNC_000001.10Chr1224,594,709224,595,510

    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)
    nssv18249379<0.001434914
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