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nsv7066592

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:88,678

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 300 SVs from 44 studies. See in: genome view    
    Submitted genomic64,627,706-64,716,383Question Mark
    Overlapping variant regions from other studies: 300 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):65,540,263-65,628,940Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066592Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr864,627,70664,716,383
    nsv7066592RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr865,540,26365,628,940

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783535inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783535Submitted genomicNC_000008.11:g.646
    27706_64716383inv
    GRCh38 (hg38)NC_000008.11Chr864,627,70664,716,383
    nssv18783535RemappedPerfectNC_000008.10:g.655
    40263_65628940inv
    GRCh37.p13First PassNC_000008.10Chr865,540,26365,628,940

    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)
    nssv187835354e-061276268
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