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nsv6740471

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:51,363

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 348 SVs from 50 studies. See in: genome view    
    Submitted genomic184,587,311-184,638,673Question Mark
    Overlapping variant regions from other studies: 348 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):185,508,465-185,559,827Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6740471Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4184,587,311184,638,673
    nsv6740471RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4185,508,465185,559,827

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18687952duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18687952Submitted genomicNC_000004.12:g.184
    587311_184638673du
    p
    GRCh38 (hg38)NC_000004.12Chr4184,587,311184,638,673
    nssv18687952RemappedPerfectNC_000004.11:g.185
    508465_185559827du
    p
    GRCh37.p13First PassNC_000004.11Chr4185,508,465185,559,827

    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)
    nssv186879524e-061272578
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