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nsv6668898

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,326

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 101 SVs from 26 studies. See in: genome view    
    Submitted genomic26,530,107-26,532,432Question Mark
    Overlapping variant regions from other studies: 101 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):26,752,975-26,755,300Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6668898Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr226,530,10726,532,432
    nsv6668898RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr226,752,97526,755,300

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18462915deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18462915Submitted genomicNC_000002.12:g.265
    30107_26532432del
    GRCh38 (hg38)NC_000002.12Chr226,530,10726,532,432
    nssv18462915RemappedPerfectNC_000002.11:g.267
    52975_26755300del
    GRCh37.p13First PassNC_000002.11Chr226,752,97526,755,300

    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)
    nssv184629151.1e-053274950
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