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nsv7068478

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,892

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 155 SVs from 37 studies. See in: genome view    
    Submitted genomic53,302,427-53,318,318Question Mark
    Overlapping variant regions from other studies: 155 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):53,696,211-53,712,102Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7068478Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1253,302,42753,318,318
    nsv7068478RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1253,696,21153,712,102

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18751952inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18751952Submitted genomicNC_000012.12:g.533
    02427_53318318inv
    GRCh38 (hg38)NC_000012.12Chr1253,302,42753,318,318
    nssv18751952RemappedPerfectNC_000012.11:g.536
    96211_53712102inv
    GRCh37.p13First PassNC_000012.11Chr1253,696,21153,712,102

    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)
    nssv187519524e-061276268
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