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nsv7038795

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,426

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 178 SVs from 15 studies. See in: genome view    
    Submitted genomic237,773,267-237,778,692Question Mark
    Overlapping variant regions from other studies: 178 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):238,681,910-238,687,335Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7038795Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2237,773,267237,778,692
    nsv7038795RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2238,681,910238,687,335

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767816inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767816Submitted genomicNC_000002.12:g.237
    773267_237778692in
    v
    GRCh38 (hg38)NC_000002.12Chr2237,773,267237,778,692
    nssv18767816RemappedPerfectNC_000002.11:g.238
    681910_238687335in
    v
    GRCh37.p13First PassNC_000002.11Chr2238,681,910238,687,335

    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)
    nssv187678164e-061276268
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