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nsv6383699

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:96,749

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 410 SVs from 66 studies. See in: genome view    
    Submitted genomic119,233,849-119,330,597Question Mark
    Overlapping variant regions from other studies: 410 SVs from 66 studies. See in: genome view    
    Remapped(Score: Perfect):120,155,004-120,251,752Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6383699Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4119,233,849119,330,597
    nsv6383699RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4120,155,004120,251,752

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18211976duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18211976Submitted genomicNC_000004.12:g.119
    233849_119330597du
    p
    GRCh38 (hg38)NC_000004.12Chr4119,233,849119,330,597
    nssv18211976RemappedPerfectNC_000004.11:g.120
    155004_120251752du
    p
    GRCh37.p13First PassNC_000004.11Chr4120,155,004120,251,752

    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)
    nssv18211976<0.001139290
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