U.S. flag

An official website of the United States government

nsv6980529

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 78 SVs from 18 studies. See in: genome view    
    Submitted genomic56,459,401-56,461,000Question Mark
    Overlapping variant regions from other studies: 78 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):56,493,313-56,494,912Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6980529Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1656,459,40156,461,000
    nsv6980529RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1656,493,31356,494,912

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18623922duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18623922Submitted genomicNC_000016.10:g.564
    59401_56461000dup
    GRCh38 (hg38)NC_000016.10Chr1656,459,40156,461,000
    nssv18623922RemappedPerfectNC_000016.9:g.5649
    3313_56494912dup
    GRCh37.p13First PassNC_000016.9Chr1656,493,31356,494,912

    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)
    nssv186239224e-061266610
    Support Center