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nsv7052163

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:120,156

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 368 SVs from 54 studies. See in: genome view    
    Submitted genomic87,535,323-87,655,478Question Mark
    Overlapping variant regions from other studies: 368 SVs from 54 studies. See in: genome view    
    Remapped(Score: Perfect):87,584,473-87,704,628Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052163Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr387,535,32387,655,478
    nsv7052163RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr387,584,47387,704,628

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18771088inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18771088Submitted genomicNC_000003.12:g.875
    35323_87655478inv
    GRCh38 (hg38)NC_000003.12Chr387,535,32387,655,478
    nssv18771088RemappedPerfectNC_000003.11:g.875
    84473_87704628inv
    GRCh37.p13First PassNC_000003.11Chr387,584,47387,704,628

    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)
    nssv187710884e-061276268
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