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nsv7039549

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:96,627

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 327 SVs from 56 studies. See in: genome view    
    Submitted genomic46,877,665-46,974,291Question Mark
    Overlapping variant regions from other studies: 327 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):47,343,337-47,439,963Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039549Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr146,877,66546,974,291
    nsv7039549RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr147,343,33747,439,963

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761044inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761044Submitted genomicNC_000001.11:g.468
    77665_46974291inv
    GRCh38 (hg38)NC_000001.11Chr146,877,66546,974,291
    nssv18761044RemappedPerfectNC_000001.10:g.473
    43337_47439963inv
    GRCh37.p13First PassNC_000001.10Chr147,343,33747,439,963

    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)
    nssv187610444e-061276268
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