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nsv6407079

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,036

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 77 SVs from 15 studies. See in: genome view    
    Submitted genomic47,279,508-47,281,543Question Mark
    Overlapping variant regions from other studies: 77 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):47,247,244-47,249,279Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6407079Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr647,279,50847,281,543
    nsv6407079RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr647,247,24447,249,279

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18144893deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18144893Submitted genomicNC_000006.12:g.472
    79508_47281543del
    GRCh38 (hg38)NC_000006.12Chr647,279,50847,281,543
    nssv18144893RemappedPerfectNC_000006.11:g.472
    47244_47249279del
    GRCh37.p13First PassNC_000006.11Chr647,247,24447,249,279

    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)
    nssv18144893<0.001138682
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