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nsv6870487

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:677,083

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1386 SVs from 77 studies. See in: genome view    
    Submitted genomic91,906,361-92,583,443Question Mark
    Overlapping variant regions from other studies: 1386 SVs from 77 studies. See in: genome view    
    Remapped(Score: Perfect):94,668,643-95,345,725Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6870487Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr991,906,36192,583,443
    nsv6870487RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr994,668,64395,345,725

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18750522duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18750522Submitted genomicNC_000009.12:g.919
    06361_92583443dup
    GRCh38 (hg38)NC_000009.12Chr991,906,36192,583,443
    nssv18750522RemappedPerfectNC_000009.11:g.946
    68643_95345725dup
    GRCh37.p13First PassNC_000009.11Chr994,668,64395,345,725

    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)
    nssv187505221.1e-053275322
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