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nsv6816731

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:178

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 106 SVs from 16 studies. See in: genome view    
    Submitted genomic90,173,895-90,174,072Question Mark
    Overlapping variant regions from other studies: 106 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):90,883,614-90,883,791Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6816731Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr690,173,89590,174,072
    nsv6816731RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr690,883,61490,883,791

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18717826duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18717826Submitted genomicNC_000006.12:g.901
    73895_90174072dup
    GRCh38 (hg38)NC_000006.12Chr690,173,89590,174,072
    nssv18717826RemappedPerfectNC_000006.11:g.908
    83614_90883791dup
    GRCh37.p13First PassNC_000006.11Chr690,883,61490,883,791

    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)
    nssv187178264e-061221696
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