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nsv6898203

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:188

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 150 SVs from 15 studies. See in: genome view    
    Submitted genomic124,631,297-124,631,484Question Mark
    Overlapping variant regions from other studies: 150 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):124,501,193-124,501,380Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6898203Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11124,631,297124,631,484
    nsv6898203RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11124,501,193124,501,380

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18581119duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18581119Submitted genomicNC_000011.10:g.124
    631297_124631484du
    p
    GRCh38 (hg38)NC_000011.10Chr11124,631,297124,631,484
    nssv18581119RemappedPerfectNC_000011.9:g.1245
    01193_124501380dup
    GRCh37.p13First PassNC_000011.9Chr11124,501,193124,501,380

    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)
    nssv185811194e-061236118
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