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nsv6711296

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,300

    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 genomic51,956,001-51,958,300Question Mark
    Overlapping variant regions from other studies: 108 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):51,990,017-51,992,316Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6711296Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr351,956,00151,958,300
    nsv6711296RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr351,990,01751,992,316

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18679074duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18679074Submitted genomicNC_000003.12:g.519
    56001_51958300dup
    GRCh38 (hg38)NC_000003.12Chr351,956,00151,958,300
    nssv18679074RemappedPerfectNC_000003.11:g.519
    90017_51992316dup
    GRCh37.p13First PassNC_000003.11Chr351,990,01751,992,316

    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)
    nssv186790748.6e-0522251364
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