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nsv7075484

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,691,931

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7749 SVs from 121 studies. See in: genome view    
    Submitted genomic48,343,569-50,035,499Question Mark
    Overlapping variant regions from other studies: 7279 SVs from 119 studies. See in: genome view    
    Remapped(Score: Pass):48,365,121-49,862,647Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7075484Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1148,343,56950,035,499
    nsv7075484RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1148,365,12149,862,647

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18736879inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18736879Submitted genomicNC_000011.10:g.483
    43569_50035499inv
    GRCh38 (hg38)NC_000011.10Chr1148,343,56950,035,499
    nssv18736879RemappedPassNC_000011.9:g.4836
    5121_49862647inv
    GRCh37.p13First PassNC_000011.9Chr1148,365,12149,862,647

    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)
    nssv187368795e-0514272242
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