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nsv6553316

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:364

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 147 SVs from 25 studies. See in: genome view    
    Submitted genomic226,294,544-226,294,907Question Mark
    Overlapping variant regions from other studies: 150 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):226,482,245-226,482,608Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6553316Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1226,294,544226,294,907
    nsv6553316RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1226,482,245226,482,608

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18249450inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18249450Submitted genomicNC_000001.11:g.226
    294544_226294907in
    v
    GRCh38 (hg38)NC_000001.11Chr1226,294,544226,294,907
    nssv18249450RemappedPerfectNC_000001.10:g.226
    482245_226482608in
    v
    GRCh37.p13First PassNC_000001.10Chr1226,482,245226,482,608

    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)
    nssv18249450<0.001733998
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