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nsv7044635

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:111

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 28 studies. See in: genome view    
    Submitted genomic33,992,774-33,992,884Question Mark
    Overlapping variant regions from other studies: 111 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):33,992,879-33,992,989Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044635Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr533,992,77433,992,884
    nsv7044635RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr533,992,87933,992,989

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18775804inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18775804Submitted genomicNC_000005.10:g.339
    92774_33992884inv
    GRCh38 (hg38)NC_000005.10Chr533,992,77433,992,884
    nssv18775804RemappedPerfectNC_000005.9:g.3399
    2879_33992989inv
    GRCh37.p13First PassNC_000005.9Chr533,992,87933,992,989

    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)
    nssv18775804<0.00148273692
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