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nsv6605539

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:75,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 616 SVs from 66 studies. See in: genome view    
    Submitted genomic159,653,701-159,728,800Question Mark
    Overlapping variant regions from other studies: 616 SVs from 66 studies. See in: genome view    
    Remapped(Score: Perfect):160,074,733-160,149,832Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6605539Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6159,653,701159,728,800
    nsv6605539RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6160,074,733160,149,832

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18216720duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18216720Submitted genomicNC_000006.12:g.159
    653701_159728800du
    p
    GRCh38 (hg38)NC_000006.12Chr6159,653,701159,728,800
    nssv18216720RemappedPerfectNC_000006.11:g.160
    074733_160149832du
    p
    GRCh37.p13First PassNC_000006.11Chr6160,074,733160,149,832

    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)
    nssv18216720<0.001339208
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