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nsv6507466

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,070

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 151 SVs from 21 studies. See in: genome view    
    Submitted genomic44,074,150-44,083,219Question Mark
    Overlapping variant regions from other studies: 149 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):42,151,518-42,160,587Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6507466Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1744,074,15044,083,219
    nsv6507466RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1742,151,51842,160,587

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18186043duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18186043Submitted genomicNC_000017.11:g.440
    74150_44083219dup
    GRCh38 (hg38)NC_000017.11Chr1744,074,15044,083,219
    nssv18186043RemappedPerfectNC_000017.10:g.421
    51518_42160587dup
    GRCh37.p13First PassNC_000017.10Chr1742,151,51842,160,587

    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)
    nssv18186043<0.001139294
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