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nsv7032059

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:685,986

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2738 SVs from 105 studies. See in: genome view    
    Submitted genomic43,207,013-43,892,998Question Mark
    Overlapping variant regions from other studies: 2740 SVs from 105 studies. See in: genome view    
    Remapped(Score: Good):44,627,123-45,312,879Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7032059Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2143,207,01343,892,998
    nsv7032059RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2144,627,12345,312,879

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18644116duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18644116Submitted genomicNC_000021.9:g.4320
    7013_43892998dup
    GRCh38 (hg38)NC_000021.9Chr2143,207,01343,892,998
    nssv18644116RemappedGoodNC_000021.8:g.4462
    7123_45312879dup
    GRCh37.p13First PassNC_000021.8Chr2144,627,12345,312,879

    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)
    nssv186441164e-061275942
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