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nsv7041292

  • 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: 120 SVs from 18 studies. See in: genome view    
    Submitted genomic143,261,141-143,261,193Question Mark
    Overlapping variant regions from other studies: 120 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):144,018,710-144,018,762Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7041292Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2143,261,141143,261,193
    nsv7041292RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2144,018,710144,018,762

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765881inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765881Submitted genomicNC_000002.12:g.143
    261141_143261193in
    v
    GRCh38 (hg38)NC_000002.12Chr2143,261,141143,261,193
    nssv18765881RemappedPerfectNC_000002.11:g.144
    018710_144018762in
    v
    GRCh37.p13First PassNC_000002.11Chr2144,018,710144,018,762

    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)
    nssv18765881<0.001220274278
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