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nsv7008357

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:45

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 119 SVs from 24 studies. See in: genome view    
    Submitted genomic3,045,426-3,045,470Question Mark
    Overlapping variant regions from other studies: 119 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):3,026,072-3,026,116Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7008357Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr203,045,4263,045,470
    nsv7008357RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr203,026,0723,026,116

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18431151deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18431151Submitted genomicNC_000020.11:g.304
    5426_3045470del
    GRCh38 (hg38)NC_000020.11Chr203,045,4263,045,470
    nssv18431151RemappedPerfectNC_000020.10:g.302
    6072_3026116del
    GRCh37.p13First PassNC_000020.10Chr203,026,0723,026,116

    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)
    nssv184311511.2e-053252744
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