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nsv7066397

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,808

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 119 SVs from 30 studies. See in: genome view    
    Submitted genomic88,080,569-88,087,376Question Mark
    Overlapping variant regions from other studies: 119 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):87,813,737-87,820,544Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066397Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1188,080,56988,087,376
    nsv7066397RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1187,813,73787,820,544

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18739696inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18739696Submitted genomicNC_000011.10:g.880
    80569_88087376inv
    GRCh38 (hg38)NC_000011.10Chr1188,080,56988,087,376
    nssv18739696RemappedPerfectNC_000011.9:g.8781
    3737_87820544inv
    GRCh37.p13First PassNC_000011.9Chr1187,813,73787,820,544

    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)
    nssv187396961.8e-055274722
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