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nsv7026265

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 131 SVs from 20 studies. See in: genome view    
    Submitted genomic29,331,301-29,336,200Question Mark
    Overlapping variant regions from other studies: 131 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):30,703,622-30,708,521Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7026265Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2129,331,30129,336,200
    nsv7026265RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2130,703,62230,708,521

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18436892deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18436892Submitted genomicNC_000021.9:g.2933
    1301_29336200del
    GRCh38 (hg38)NC_000021.9Chr2129,331,30129,336,200
    nssv18436892RemappedPerfectNC_000021.8:g.3070
    3622_30708521del
    GRCh37.p13First PassNC_000021.8Chr2130,703,62230,708,521

    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)
    nssv184368924e-061276176
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