U.S. flag

An official website of the United States government

nsv6653221

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:87,924

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 405 SVs from 57 studies. See in: genome view    
    Submitted genomic6,616,965-6,704,888Question Mark
    Overlapping variant regions from other studies: 405 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):6,677,025-6,764,948Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6653221Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr16,616,9656,704,888
    nsv6653221RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr16,677,0256,764,948

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18629602duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18629602Submitted genomicNC_000001.11:g.661
    6965_6704888dup
    GRCh38 (hg38)NC_000001.11Chr16,616,9656,704,888
    nssv18629602RemappedPerfectNC_000001.10:g.667
    7025_6764948dup
    GRCh37.p13First PassNC_000001.10Chr16,677,0256,764,948

    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)
    nssv186296024e-061275364
    Support Center