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nsv6989378

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:55,273

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 302 SVs from 37 studies. See in: genome view    
    Submitted genomic49,006,578-49,061,850Question Mark
    Overlapping variant regions from other studies: 300 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):47,083,940-47,139,212Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6989378Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1749,006,57849,061,850
    nsv6989378RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1747,083,94047,139,212

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18626615duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18626615Submitted genomicNC_000017.11:g.490
    06578_49061850dup
    GRCh38 (hg38)NC_000017.11Chr1749,006,57849,061,850
    nssv18626615RemappedPerfectNC_000017.10:g.470
    83940_47139212dup
    GRCh37.p13First PassNC_000017.10Chr1747,083,94047,139,212

    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)
    nssv186266151.4e-054275622
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