U.S. flag

An official website of the United States government

nsv7041974

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,792

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 130 SVs from 27 studies. See in: genome view    
    Submitted genomic158,025,179-158,040,970Question Mark
    Overlapping variant regions from other studies: 134 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):157,994,969-158,010,760Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7041974Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1158,025,179158,040,970
    nsv7041974RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1157,994,969158,010,760

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18747376inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18747376Submitted genomicNC_000001.11:g.158
    025179_158040970in
    v
    GRCh38 (hg38)NC_000001.11Chr1158,025,179158,040,970
    nssv18747376RemappedPerfectNC_000001.10:g.157
    994969_158010760in
    v
    GRCh37.p13First PassNC_000001.10Chr1157,994,969158,010,760

    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)
    nssv187473764e-061276268
    Support Center