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nsv6783042

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:53

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 133 SVs from 18 studies. See in: genome view    
    Submitted genomic4,086,101-4,086,153Question Mark
    Overlapping variant regions from other studies: 133 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):4,086,335-4,086,387Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6783042Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr64,086,1014,086,153
    nsv6783042RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr64,086,3354,086,387

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18715439duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18715439Submitted genomicNC_000006.12:g.408
    6101_4086153dup
    GRCh38 (hg38)NC_000006.12Chr64,086,1014,086,153
    nssv18715439RemappedPerfectNC_000006.11:g.408
    6335_4086387dup
    GRCh37.p13First PassNC_000006.11Chr64,086,3354,086,387

    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)
    nssv18715439<0.001132218254
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