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nsv6884712

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:51,442

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 230 SVs from 47 studies. See in: genome view    
    Submitted genomic27,713,355-27,764,796Question Mark
    Overlapping variant regions from other studies: 230 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):28,002,284-28,053,725Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6884712Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1027,713,35527,764,796
    nsv6884712RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1028,002,28428,053,725

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18588191duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18588191Submitted genomicNC_000010.11:g.277
    13355_27764796dup
    GRCh38 (hg38)NC_000010.11Chr1027,713,35527,764,796
    nssv18588191RemappedPerfectNC_000010.10:g.280
    02284_28053725dup
    GRCh37.p13First PassNC_000010.10Chr1028,002,28428,053,725

    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)
    nssv185881914e-061275270
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