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nsv6652673

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:67,487

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 436 SVs from 60 studies. See in: genome view    
    Submitted genomic6,520,417-6,587,903Question Mark
    Overlapping variant regions from other studies: 436 SVs from 60 studies. See in: genome view    
    Remapped(Score: Perfect):6,580,477-6,647,963Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6652673Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr16,520,4176,587,903
    nsv6652673RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr16,580,4776,647,963

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18629560duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18629560Submitted genomicNC_000001.11:g.652
    0417_6587903dup
    GRCh38 (hg38)NC_000001.11Chr16,520,4176,587,903
    nssv18629560RemappedPerfectNC_000001.10:g.658
    0477_6647963dup
    GRCh37.p13First PassNC_000001.10Chr16,580,4776,647,963

    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)
    nssv186295604e-061275880
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