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nsv7042155

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:53

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 128 SVs from 19 studies. See in: genome view    
    Submitted genomic191,150,217-191,150,269Question Mark
    Overlapping variant regions from other studies: 128 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):192,014,943-192,014,995Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7042155Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2191,150,217191,150,269
    nsv7042155RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2192,014,943192,014,995

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18766579inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18766579Submitted genomicNC_000002.12:g.191
    150217_191150269in
    v
    GRCh38 (hg38)NC_000002.12Chr2191,150,217191,150,269
    nssv18766579RemappedPerfectNC_000002.11:g.192
    014943_192014995in
    v
    GRCh37.p13First PassNC_000002.11Chr2192,014,943192,014,995

    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)
    nssv187665794e-061276256
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