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nsv6976565

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:779

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 131 SVs from 31 studies. See in: genome view    
    Submitted genomic86,030,043-86,030,821Question Mark
    Overlapping variant regions from other studies: 131 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):86,496,387-86,497,165Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6976565Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1486,030,04386,030,821
    nsv6976565RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1486,496,38786,497,165

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18615073duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18615073Submitted genomicNC_000014.9:g.8603
    0043_86030821dup
    GRCh38 (hg38)NC_000014.9Chr1486,030,04386,030,821
    nssv18615073RemappedPerfectNC_000014.8:g.8649
    6387_86497165dup
    GRCh37.p13First PassNC_000014.8Chr1486,496,38786,497,165

    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)
    nssv186150734e-061251474
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