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nsv6969355

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:41,268

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 312 SVs from 57 studies. See in: genome view    
    Submitted genomic3,121,230-3,162,497Question Mark
    Overlapping variant regions from other studies: 312 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):3,171,231-3,212,498Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6969355Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr163,121,2303,162,497
    nsv6969355RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr163,171,2313,212,498

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18399053deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18399053Submitted genomicNC_000016.10:g.312
    1230_3162497del
    GRCh38 (hg38)NC_000016.10Chr163,121,2303,162,497
    nssv18399053RemappedPerfectNC_000016.9:g.3171
    231_3212498del
    GRCh37.p13First PassNC_000016.9Chr163,171,2313,212,498

    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)
    nssv183990534e-061274462
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