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nsv6913749

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,232

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 123 SVs from 42 studies. See in: genome view    
    Submitted genomic5,339,887-5,351,118Question Mark
    Overlapping variant regions from other studies: 123 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):5,361,117-5,372,348Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6913749Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr115,339,8875,351,118
    nsv6913749RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr115,361,1175,372,348

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18352650deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18352650Submitted genomicNC_000011.10:g.533
    9887_5351118del
    GRCh38 (hg38)NC_000011.10Chr115,339,8875,351,118
    nssv18352650RemappedPerfectNC_000011.9:g.5361
    117_5372348del
    GRCh37.p13First PassNC_000011.9Chr115,361,1175,372,348

    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)
    nssv183526501.1e-053276232
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