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nsv6656636

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 113 SVs from 21 studies. See in: genome view    
    Submitted genomic92,838,901-92,840,500Question Mark
    Overlapping variant regions from other studies: 113 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):93,304,458-93,306,057Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6656636Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr192,838,90192,840,500
    nsv6656636RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr193,304,45893,306,057

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18639079duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18639079Submitted genomicNC_000001.11:g.928
    38901_92840500dup
    GRCh38 (hg38)NC_000001.11Chr192,838,90192,840,500
    nssv18639079RemappedPerfectNC_000001.10:g.933
    04458_93306057dup
    GRCh37.p13First PassNC_000001.10Chr193,304,45893,306,057

    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)
    nssv186390794e-061268410
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