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nsv6461169

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,983

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 108 SVs from 26 studies. See in: genome view    
    Submitted genomic66,521,958-66,524,940Question Mark
    Overlapping variant regions from other studies: 108 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):66,289,429-66,292,411Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6461169Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1166,521,95866,524,940
    nsv6461169RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1166,289,42966,292,411

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17992574deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17992574Submitted genomicNC_000011.10:g.665
    21958_66524940del
    GRCh38 (hg38)NC_000011.10Chr1166,521,95866,524,940
    nssv17992574RemappedPerfectNC_000011.9:g.6628
    9429_66292411del
    GRCh37.p13First PassNC_000011.9Chr1166,289,42966,292,411

    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)
    nssv17992574<0.001139134
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