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nsv6991511

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19,865

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 332 SVs from 52 studies. See in: genome view    
    Submitted genomic89,532,677-89,552,541Question Mark
    Overlapping variant regions from other studies: 332 SVs from 52 studies. See in: genome view    
    Remapped(Score: Perfect):89,599,085-89,618,949Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6991511Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1689,532,67789,552,541
    nsv6991511RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1689,599,08589,618,949

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18624960duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18624960Submitted genomicNC_000016.10:g.895
    32677_89552541dup
    GRCh38 (hg38)NC_000016.10Chr1689,532,67789,552,541
    nssv18624960RemappedPerfectNC_000016.9:g.8959
    9085_89618949dup
    GRCh37.p13First PassNC_000016.9Chr1689,599,08589,618,949

    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)
    nssv186249604e-061276192
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