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nsv7051835

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,465

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 136 SVs from 32 studies. See in: genome view    
    Submitted genomic133,054,944-133,057,408Question Mark
    Overlapping variant regions from other studies: 136 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):133,812,517-133,814,981Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7051835Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2133,054,944133,057,408
    nsv7051835RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2133,812,517133,814,981

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765738inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765738Submitted genomicNC_000002.12:g.133
    054944_133057408in
    v
    GRCh38 (hg38)NC_000002.12Chr2133,054,944133,057,408
    nssv18765738RemappedPerfectNC_000002.11:g.133
    812517_133814981in
    v
    GRCh37.p13First PassNC_000002.11Chr2133,812,517133,814,981

    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)
    nssv187657387e-062275084
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