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nsv7024691

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 171 SVs from 24 studies. See in: genome view    
    Submitted genomic14,376,301-14,377,900Question Mark
    Overlapping variant regions from other studies: 171 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):15,748,622-15,750,221Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7024691Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2114,376,30114,377,900
    nsv7024691RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2115,748,62215,750,221

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18645107duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18645107Submitted genomicNC_000021.9:g.1437
    6301_14377900dup
    GRCh38 (hg38)NC_000021.9Chr2114,376,30114,377,900
    nssv18645107RemappedPerfectNC_000021.8:g.1574
    8622_15750221dup
    GRCh37.p13First PassNC_000021.8Chr2115,748,62215,750,221

    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)
    nssv18645107<0.0012263494
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