U.S. flag

An official website of the United States government

nsv7056510

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,727

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 112 SVs from 32 studies. See in: genome view    
    Submitted genomic86,697,455-86,709,181Question Mark
    Overlapping variant regions from other studies: 112 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):86,326,771-86,338,497Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7056510Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr786,697,45586,709,181
    nsv7056510RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr786,326,77186,338,497

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18782910inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18782910Submitted genomicNC_000007.14:g.866
    97455_86709181inv
    GRCh38 (hg38)NC_000007.14Chr786,697,45586,709,181
    nssv18782910RemappedPerfectNC_000007.13:g.863
    26771_86338497inv
    GRCh37.p13First PassNC_000007.13Chr786,326,77186,338,497

    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)
    nssv187829107e-062274886
    Support Center