U.S. flag

An official website of the United States government

nsv7053924

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:170,637

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 446 SVs from 55 studies. See in: genome view    
    Submitted genomic203,102,071-203,272,707Question Mark
    Overlapping variant regions from other studies: 446 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):203,071,199-203,241,835Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7053924Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1203,102,071203,272,707
    nsv7053924RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1203,071,199203,241,835

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18741326inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18741326Submitted genomicNC_000001.11:g.203
    102071_203272707in
    v
    GRCh38 (hg38)NC_000001.11Chr1203,102,071203,272,707
    nssv18741326RemappedPerfectNC_000001.10:g.203
    071199_203241835in
    v
    GRCh37.p13First PassNC_000001.10Chr1203,071,199203,241,835

    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)
    nssv187413264e-061276268
    Support Center