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nsv7037889

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:214,694

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 957 SVs from 62 studies. See in: genome view    
    Submitted genomic25,958,144-26,172,837Question Mark
    Overlapping variant regions from other studies: 966 SVs from 62 studies. See in: genome view    
    Remapped(Score: Good):27,330,458-27,545,155Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7037889Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2125,958,14426,172,837
    nsv7037889RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2127,330,45827,545,155

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18646472duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18646472Submitted genomicNC_000021.9:g.2595
    8144_26172837dup
    GRCh38 (hg38)NC_000021.9Chr2125,958,14426,172,837
    nssv18646472RemappedGoodNC_000021.8:g.2733
    0458_27545155dup
    GRCh37.p13First PassNC_000021.8Chr2127,330,45827,545,155

    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)
    nssv186464727e-062275706
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