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nsv6560305

  • 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 19 studies. See in: genome view    
    Submitted genomic137,146,041-137,146,716Question Mark
    Overlapping variant regions from other studies: 104 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):137,467,178-137,467,853Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6560305Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6137,146,041137,146,716
    nsv6560305RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6137,467,178137,467,853

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18272418inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18272418Submitted genomicNC_000006.12:g.137
    146041_137146716in
    v
    GRCh38 (hg38)NC_000006.12Chr6137,146,041137,146,716
    nssv18272418RemappedPerfectNC_000006.11:g.137
    467178_137467853in
    v
    GRCh37.p13First PassNC_000006.11Chr6137,467,178137,467,853

    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)
    nssv18272418<0.001135652
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