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nsv6739536

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:349

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 119 SVs from 26 studies. See in: genome view    
    Submitted genomic67,706,865-67,707,213Question Mark
    Overlapping variant regions from other studies: 119 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):68,572,583-68,572,931Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6739536Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr467,706,86567,707,213
    nsv6739536RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr468,572,58368,572,931

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18692013duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18692013Submitted genomicNC_000004.12:g.677
    06865_67707213dup
    GRCh38 (hg38)NC_000004.12Chr467,706,86567,707,213
    nssv18692013RemappedPerfectNC_000004.11:g.685
    72583_68572931dup
    GRCh37.p13First PassNC_000004.11Chr468,572,58368,572,931

    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)
    nssv186920134e-061243598
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