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nsv6808361

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:108

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 109 SVs from 18 studies. See in: genome view    
    Submitted genomic110,460,428-110,460,535Question Mark
    Overlapping variant regions from other studies: 109 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):110,781,631-110,781,738Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6808361Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6110,460,428110,460,535
    nsv6808361RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6110,781,631110,781,738

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18709043duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18709043Submitted genomicNC_000006.12:g.110
    460428_110460535du
    p
    GRCh38 (hg38)NC_000006.12Chr6110,460,428110,460,535
    nssv18709043RemappedPerfectNC_000006.11:g.110
    781631_110781738du
    p
    GRCh37.p13First PassNC_000006.11Chr6110,781,631110,781,738

    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)
    nssv187090434e-061223220
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