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nsv7057550

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,792

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 90 SVs from 22 studies. See in: genome view    
    Submitted genomic228,067,349-228,072,140Question Mark
    Overlapping variant regions from other studies: 90 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):228,932,065-228,936,856Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7057550Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2228,067,349228,072,140
    nsv7057550RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2228,932,065228,936,856

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767675inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767675Submitted genomicNC_000002.12:g.228
    067349_228072140in
    v
    GRCh38 (hg38)NC_000002.12Chr2228,067,349228,072,140
    nssv18767675RemappedPerfectNC_000002.11:g.228
    932065_228936856in
    v
    GRCh37.p13First PassNC_000002.11Chr2228,932,065228,936,856

    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)
    nssv187676757e-062276268
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