U.S. flag

An official website of the United States government

nsv7063761

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,479,681

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7080 SVs from 119 studies. See in: genome view    
    Submitted genomic48,467,658-49,947,338Question Mark
    Overlapping variant regions from other studies: 6814 SVs from 117 studies. See in: genome view    
    Remapped(Score: Pass):48,489,210-49,862,647Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7063761Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1148,467,65849,947,338
    nsv7063761RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1148,489,21049,862,647

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18731175inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18731175Submitted genomicNC_000011.10:g.484
    67658_49947338inv
    GRCh38 (hg38)NC_000011.10Chr1148,467,65849,947,338
    nssv18731175RemappedPassNC_000011.9:g.4848
    9210_49862647inv
    GRCh37.p13First PassNC_000011.9Chr1148,489,21049,862,647

    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)
    nssv187311754e-061276268
    Support Center