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nsv6908087

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,866

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 181 SVs from 42 studies. See in: genome view    
    Submitted genomic106,259,284-106,278,149Question Mark
    Overlapping variant regions from other studies: 181 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):106,130,011-106,148,876Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6908087Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11106,259,284106,278,149
    nsv6908087RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11106,130,011106,148,876

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18588649duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18588649Submitted genomicNC_000011.10:g.106
    259284_106278149du
    p
    GRCh38 (hg38)NC_000011.10Chr11106,259,284106,278,149
    nssv18588649RemappedPerfectNC_000011.9:g.1061
    30011_106148876dup
    GRCh37.p13First PassNC_000011.9Chr11106,130,011106,148,876

    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)
    nssv185886494e-061275954
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