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nsv6989369

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:958,833

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3504 SVs from 93 studies. See in: genome view    
    Submitted genomic1,348,499-2,307,331Question Mark
    Overlapping variant regions from other studies: 3504 SVs from 93 studies. See in: genome view    
    Remapped(Score: Perfect):1,348,500-2,307,330Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6989369Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr181,348,4992,307,331
    nsv6989369RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr181,348,5002,307,330

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18631029duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18631029Submitted genomicNC_000018.10:g.134
    8499_2307331dup
    GRCh38 (hg38)NC_000018.10Chr181,348,4992,307,331
    nssv18631029RemappedPerfectNC_000018.9:g.1348
    500_2307330dup
    GRCh37.p13First PassNC_000018.9Chr181,348,5002,307,330

    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)
    nssv186310294e-061269994
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