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nsv6700836

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,147,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8194 SVs from 107 studies. See in: genome view    
    Submitted genomic48,056,801-51,204,000Question Mark
    Overlapping variant regions from other studies: 8176 SVs from 107 studies. See in: genome view    
    Remapped(Score: Good):48,098,291-51,241,431Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6700836Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr348,056,80151,204,000
    nsv6700836RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr348,098,29151,241,431

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18480639deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18480639Submitted genomicNC_000003.12:g.480
    56801_51204000del
    GRCh38 (hg38)NC_000003.12Chr348,056,80151,204,000
    nssv18480639RemappedGoodNC_000003.11:g.480
    98291_51241431del
    GRCh37.p13First PassNC_000003.11Chr348,098,29151,241,431

    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)
    nssv184806398e-062252138
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