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nsv6918063

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:219

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 72 SVs from 21 studies. See in: genome view    
    Submitted genomic6,002,366-6,002,584Question Mark
    Overlapping variant regions from other studies: 72 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):6,023,596-6,023,814Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6918063Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr116,002,3666,002,584
    nsv6918063RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr116,023,5966,023,814

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18584385duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18584385Submitted genomicNC_000011.10:g.600
    2366_6002584dup
    GRCh38 (hg38)NC_000011.10Chr116,002,3666,002,584
    nssv18584385RemappedPerfectNC_000011.9:g.6023
    596_6023814dup
    GRCh37.p13First PassNC_000011.9Chr116,023,5966,023,814

    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)
    nssv185843854e-061218980
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