U.S. flag

An official website of the United States government

nsv6831197

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:181,435

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 557 SVs from 68 studies. See in: genome view    
    Submitted genomic64,520,099-64,701,533Question Mark
    Overlapping variant regions from other studies: 565 SVs from 68 studies. See in: genome view    
    Remapped(Score: Perfect):63,980,477-64,161,911Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6831197Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr764,520,09964,701,533
    nsv6831197RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr763,980,47764,161,911

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18726568duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18726568Submitted genomicNC_000007.14:g.645
    20099_64701533dup
    GRCh38 (hg38)NC_000007.14Chr764,520,09964,701,533
    nssv18726568RemappedPerfectNC_000007.13:g.639
    80477_64161911dup
    GRCh37.p13First PassNC_000007.13Chr763,980,47764,161,911

    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)
    nssv187265684.3e-0512272296
    Support Center