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nsv6886834

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,896,014

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 15891 SVs from 134 studies. See in: genome view    
    Submitted genomic45,568,878-51,464,891Question Mark
    Overlapping variant regions from other studies: 15160 SVs from 133 studies. See in: genome view    
    Remapped(Score: Pass):46,064,326-53,224,651Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6886834Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1045,568,87851,464,891
    nsv6886834RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1046,064,32653,224,651

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18336626deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18336626Submitted genomicNC_000010.11:g.455
    68878_51464891del
    GRCh38 (hg38)NC_000010.11Chr1045,568,87851,464,891
    nssv18336626RemappedPassNC_000010.10:g.460
    64326_53224651del
    GRCh37.p13First PassNC_000010.10Chr1046,064,32653,224,651

    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)
    nssv183366264.3e-0511251766
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