U.S. flag

An official website of the United States government

nsv7064092

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:158

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 108 SVs from 25 studies. See in: genome view    
    Submitted genomic88,052,535-88,052,692Question Mark
    Overlapping variant regions from other studies: 108 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):87,785,703-87,785,860Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7064092Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1188,052,53588,052,692
    nsv7064092RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1187,785,70387,785,860

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18734778inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18734778Submitted genomicNC_000011.10:g.880
    52535_88052692inv
    GRCh38 (hg38)NC_000011.10Chr1188,052,53588,052,692
    nssv18734778RemappedPerfectNC_000011.9:g.8778
    5703_87785860inv
    GRCh37.p13First PassNC_000011.9Chr1187,785,70387,785,860

    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)
    nssv187347784.6e-0512274186
    Support Center