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nsv6876883

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:379,833

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2081 SVs from 86 studies. See in: genome view    
    Submitted genomic144,025,878-144,405,710Question Mark
    Overlapping variant regions from other studies: 1954 SVs from 87 studies. See in: genome view    
    Remapped(Score: Pass):145,091,982-145,631,103Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6876883Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8144,025,878144,405,710
    nsv6876883RemappedPassGRCh37.p13Primary AssemblySecond PassNC_000008.10Chr8145,091,982145,631,103

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18734823duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18734823Submitted genomicNC_000008.11:g.144
    025878_144405710du
    p
    GRCh38 (hg38)NC_000008.11Chr8144,025,878144,405,710
    nssv18734823RemappedPassNC_000008.10:g.145
    091982_145631103du
    p
    GRCh37.p13Second PassNC_000008.10Chr8145,091,982145,631,103

    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)
    nssv187348234e-061271052
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