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nsv6930563

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:449,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1279 SVs from 62 studies. See in: genome view    
    Submitted genomic27,129,201-27,579,100Question Mark
    Overlapping variant regions from other studies: 1279 SVs from 62 studies. See in: genome view    
    Remapped(Score: Perfect):27,703,338-28,153,237Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6930563Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1327,129,20127,579,100
    nsv6930563RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1327,703,33828,153,237

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18600773duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18600773Submitted genomicNC_000013.11:g.271
    29201_27579100dup
    GRCh38 (hg38)NC_000013.11Chr1327,129,20127,579,100
    nssv18600773RemappedPerfectNC_000013.10:g.277
    03338_28153237dup
    GRCh37.p13First PassNC_000013.10Chr1327,703,33828,153,237

    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)
    nssv186007737e-062273680
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