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nsv6900564

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:223

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 22 studies. See in: genome view    
    Submitted genomic106,264,311-106,264,533Question Mark
    Overlapping variant regions from other studies: 115 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):106,135,038-106,135,260Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6900564Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11106,264,311106,264,533
    nsv6900564RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11106,135,038106,135,260

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18579823duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18579823Submitted genomicNC_000011.10:g.106
    264311_106264533du
    p
    GRCh38 (hg38)NC_000011.10Chr11106,264,311106,264,533
    nssv18579823RemappedPerfectNC_000011.9:g.1061
    35038_106135260dup
    GRCh37.p13First PassNC_000011.9Chr11106,135,038106,135,260

    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)
    nssv185798238e-062238550
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