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nsv6459035

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,926

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 236 SVs from 44 studies. See in: genome view    
    Submitted genomic124,208,803-124,225,728Question Mark
    Overlapping variant regions from other studies: 237 SVs from 44 studies. See in: genome view    
    Remapped(Score: Good):124,079,510-124,096,433Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6459035Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11124,208,803124,225,728
    nsv6459035RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11124,079,510124,096,433

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18185577duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18185577Submitted genomicNC_000011.10:g.124
    208803_124225728du
    p
    GRCh38 (hg38)NC_000011.10Chr11124,208,803124,225,728
    nssv18185577RemappedGoodNC_000011.9:g.1240
    79510_124096433dup
    GRCh37.p13First PassNC_000011.9Chr11124,079,510124,096,433

    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)
    nssv18185577<0.001235772
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