U.S. flag

An official website of the United States government

nsv7038217

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,203,803

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 18357 SVs from 119 studies. See in: genome view    
    Submitted genomic142,898,166-151,101,968Question Mark
    Overlapping variant regions from other studies: 18357 SVs from 119 studies. See in: genome view    
    Remapped(Score: Perfect):142,277,731-150,481,529Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7038217Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5142,898,166151,101,968
    nsv7038217RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5142,277,731150,481,529

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18775121inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18775121Submitted genomicNC_000005.10:g.142
    898166_151101968in
    v
    GRCh38 (hg38)NC_000005.10Chr5142,898,166151,101,968
    nssv18775121RemappedPerfectNC_000005.9:g.1422
    77731_150481529inv
    GRCh37.p13First PassNC_000005.9Chr5142,277,731150,481,529

    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)
    nssv187751214e-061276268
    Support Center