U.S. flag

An official website of the United States government

nsv7075597

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19,287

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 201 SVs from 56 studies. See in: genome view    
    Submitted genomic68,033,455-68,052,741Question Mark
    Overlapping variant regions from other studies: 201 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):67,800,922-67,820,208Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7075597Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1168,033,45568,052,741
    nsv7075597RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1167,800,92267,820,208

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18743545inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18743545Submitted genomicNC_000011.10:g.680
    33455_68052741inv
    GRCh38 (hg38)NC_000011.10Chr1168,033,45568,052,741
    nssv18743545RemappedPerfectNC_000011.9:g.6780
    0922_67820208inv
    GRCh37.p13First PassNC_000011.9Chr1167,800,92267,820,208

    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)
    nssv187435452.5e-057274760
    Support Center