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nsv7044499

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,764,299

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4153 SVs from 91 studies. See in: genome view    
    Submitted genomic16,435,218-18,199,516Question Mark
    Overlapping variant regions from other studies: 4153 SVs from 91 studies. See in: genome view    
    Remapped(Score: Perfect):16,436,841-18,201,139Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044499Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr416,435,21818,199,516
    nsv7044499RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr416,436,84118,201,139

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18773131inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18773131Submitted genomicNC_000004.12:g.164
    35218_18199516inv
    GRCh38 (hg38)NC_000004.12Chr416,435,21818,199,516
    nssv18773131RemappedPerfectNC_000004.11:g.164
    36841_18201139inv
    GRCh37.p13First PassNC_000004.11Chr416,436,84118,201,139

    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)
    nssv187731311.1e-053275946
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