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nsv6553679

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,805

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 127 SVs from 22 studies. See in: genome view    
    Submitted genomic45,879,601-45,885,405Question Mark
    Overlapping variant regions from other studies: 127 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):44,508,240-44,514,044Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6553679Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2045,879,60145,885,405
    nsv6553679RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2044,508,24044,514,044

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18068365deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18068365Submitted genomicNC_000020.11:g.458
    79601_45885405del
    GRCh38 (hg38)NC_000020.11Chr2045,879,60145,885,405
    nssv18068365RemappedPerfectNC_000020.10:g.445
    08240_44514044del
    GRCh37.p13First PassNC_000020.10Chr2044,508,24044,514,044

    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)
    nssv18068365<0.001139196
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