U.S. flag

An official website of the United States government

nsv6984857

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,005

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 133 SVs from 18 studies. See in: genome view    
    Submitted genomic49,000,459-49,001,463Question Mark
    Overlapping variant regions from other studies: 131 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):47,077,821-47,078,825Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6984857Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1749,000,45949,001,463
    nsv6984857RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1747,077,82147,078,825

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18626613duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18626613Submitted genomicNC_000017.11:g.490
    00459_49001463dup
    GRCh38 (hg38)NC_000017.11Chr1749,000,45949,001,463
    nssv18626613RemappedPerfectNC_000017.10:g.470
    77821_47078825dup
    GRCh37.p13First PassNC_000017.10Chr1747,077,82147,078,825

    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)
    nssv186266138e-062257910
    Support Center