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nsv6928085

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

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 82 SVs from 17 studies. See in: genome view    
    Submitted genomic27,589,901-27,590,800Question Mark
    Overlapping variant regions from other studies: 82 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):28,164,038-28,164,937Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6928085Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1327,589,90127,590,800
    nsv6928085RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1328,164,03828,164,937

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18600107duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18600107Submitted genomicNC_000013.11:g.275
    89901_27590800dup
    GRCh38 (hg38)NC_000013.11Chr1327,589,90127,590,800
    nssv18600107RemappedPerfectNC_000013.10:g.281
    64038_28164937dup
    GRCh37.p13First PassNC_000013.10Chr1328,164,03828,164,937

    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)
    nssv186001074e-061258118
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