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nsv6752742

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 145 SVs from 29 studies. See in: genome view    
    Submitted genomic140,492,401-140,496,800Question Mark
    Overlapping variant regions from other studies: 145 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):141,413,555-141,417,954Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6752742Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4140,492,401140,496,800
    nsv6752742RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4141,413,555141,417,954

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18684581duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18684581Submitted genomicNC_000004.12:g.140
    492401_140496800du
    p
    GRCh38 (hg38)NC_000004.12Chr4140,492,401140,496,800
    nssv18684581RemappedPerfectNC_000004.11:g.141
    413555_141417954du
    p
    GRCh37.p13First PassNC_000004.11Chr4141,413,555141,417,954

    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)
    nssv18684581<0.00148262386
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