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nsv6748331

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 208 SVs from 45 studies. See in: genome view    
    Submitted genomic68,092,101-68,099,100Question Mark
    Overlapping variant regions from other studies: 208 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):68,957,819-68,964,818Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6748331Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr468,092,10168,099,100
    nsv6748331RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr468,957,81968,964,818

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18692644duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18692644Submitted genomicNC_000004.12:g.680
    92101_68099100dup
    GRCh38 (hg38)NC_000004.12Chr468,092,10168,099,100
    nssv18692644RemappedPerfectNC_000004.11:g.689
    57819_68964818dup
    GRCh37.p13First PassNC_000004.11Chr468,957,81968,964,818

    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)
    nssv186926443.2e-059272862
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