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nsv6830537

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:366

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 88 SVs from 21 studies. See in: genome view    
    Submitted genomic86,839,906-86,840,271Question Mark
    Overlapping variant regions from other studies: 88 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):86,469,222-86,469,587Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6830537Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr786,839,90686,840,271
    nsv6830537RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr786,469,22286,469,587

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18726161duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18726161Submitted genomicNC_000007.14:g.868
    39906_86840271dup
    GRCh38 (hg38)NC_000007.14Chr786,839,90686,840,271
    nssv18726161RemappedPerfectNC_000007.13:g.864
    69222_86469587dup
    GRCh37.p13First PassNC_000007.13Chr786,469,22286,469,587

    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)
    nssv187261614e-061233926
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