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nsv7055296

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:207,902

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 641 SVs from 58 studies. See in: genome view    
    Submitted genomic23,417,472-23,625,373Question Mark
    Overlapping variant regions from other studies: 641 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):23,417,581-23,625,482Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7055296Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr523,417,47223,625,373
    nsv7055296RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr523,417,58123,625,482

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18775050inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18775050Submitted genomicNC_000005.10:g.234
    17472_23625373inv
    GRCh38 (hg38)NC_000005.10Chr523,417,47223,625,373
    nssv18775050RemappedPerfectNC_000005.9:g.2341
    7581_23625482inv
    GRCh37.p13First PassNC_000005.9Chr523,417,58123,625,482

    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)
    nssv18775050<0.00128270416
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