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nsv6814097

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:912,662

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2696 SVs from 100 studies. See in: genome view    
    Submitted genomic16,798,427-17,711,088Question Mark
    Overlapping variant regions from other studies: 2696 SVs from 100 studies. See in: genome view    
    Remapped(Score: Perfect):16,838,051-17,750,712Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6814097Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr716,798,42717,711,088
    nsv6814097RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr716,838,05117,750,712

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18723518duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18723518Submitted genomicNC_000007.14:g.167
    98427_17711088dup
    GRCh38 (hg38)NC_000007.14Chr716,798,42717,711,088
    nssv18723518RemappedPerfectNC_000007.13:g.168
    38051_17750712dup
    GRCh37.p13First PassNC_000007.13Chr716,838,05117,750,712

    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)
    nssv187235181.4e-054274622
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