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nsv6706233

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 108 SVs from 27 studies. See in: genome view    
    Submitted genomic51,956,201-51,957,200Question Mark
    Overlapping variant regions from other studies: 108 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):51,990,217-51,991,216Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6706233Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr351,956,20151,957,200
    nsv6706233RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr351,990,21751,991,216

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18679075duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18679075Submitted genomicNC_000003.12:g.519
    56201_51957200dup
    GRCh38 (hg38)NC_000003.12Chr351,956,20151,957,200
    nssv18679075RemappedPerfectNC_000003.11:g.519
    90217_51991216dup
    GRCh37.p13First PassNC_000003.11Chr351,990,21751,991,216

    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)
    nssv186790758e-062237618
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