U.S. flag

An official website of the United States government

nsv6894922

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,420,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4563 SVs from 107 studies. See in: genome view    
    Submitted genomic53,112,294-54,532,893Question Mark
    Overlapping variant regions from other studies: 4567 SVs from 107 studies. See in: genome view    
    Remapped(Score: Perfect):54,872,054-56,292,653Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6894922Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1053,112,29454,532,893
    nsv6894922RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1054,872,05456,292,653

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18337094deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18337094Submitted genomicNC_000010.11:g.531
    12294_54532893del
    GRCh38 (hg38)NC_000010.11Chr1053,112,29454,532,893
    nssv18337094RemappedPerfectNC_000010.10:g.548
    72054_56292653del
    GRCh37.p13First PassNC_000010.10Chr1054,872,05456,292,653

    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)
    nssv183370944e-061274854
    Support Center