U.S. flag

An official website of the United States government

nsv7039635

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,809

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 137 SVs from 26 studies. See in: genome view    
    Submitted genomic191,160,511-191,166,319Question Mark
    Overlapping variant regions from other studies: 137 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):192,025,237-192,031,045Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039635Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2191,160,511191,166,319
    nsv7039635RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2192,025,237192,031,045

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18766580inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18766580Submitted genomicNC_000002.12:g.191
    160511_191166319in
    v
    GRCh38 (hg38)NC_000002.12Chr2191,160,511191,166,319
    nssv18766580RemappedPerfectNC_000002.11:g.192
    025237_192031045in
    v
    GRCh37.p13First PassNC_000002.11Chr2192,025,237192,031,045

    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)
    nssv187665801.1e-053276128
    Support Center