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nsv6550326

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,085

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 149 SVs from 26 studies. See in: genome view    
    Submitted genomic226,236,462-226,237,546Question Mark
    Overlapping variant regions from other studies: 152 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):226,424,163-226,425,247Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6550326Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1226,236,462226,237,546
    nsv6550326RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1226,424,163226,425,247

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18249444inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18249444Submitted genomicNC_000001.11:g.226
    236462_226237546in
    v
    GRCh38 (hg38)NC_000001.11Chr1226,236,462226,237,546
    nssv18249444RemappedPerfectNC_000001.10:g.226
    424163_226425247in
    v
    GRCh37.p13First PassNC_000001.10Chr1226,424,163226,425,247

    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)
    nssv18249444<0.001634174
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