U.S. flag

An official website of the United States government

nsv6540450

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:617

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 190 SVs from 19 studies. See in: genome view    
    Submitted genomic238,070,470-238,071,086Question Mark
    Overlapping variant regions from other studies: 190 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):238,979,111-238,979,727Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6540450Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2238,070,470238,071,086
    nsv6540450RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2238,979,111238,979,727

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18257433inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18257433Submitted genomicNC_000002.12:g.238
    070470_238071086in
    v
    GRCh38 (hg38)NC_000002.12Chr2238,070,470238,071,086
    nssv18257433RemappedPerfectNC_000002.11:g.238
    979111_238979727in
    v
    GRCh37.p13First PassNC_000002.11Chr2238,979,111238,979,727

    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)
    nssv18257433<0.001135442
    Support Center