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nsv6722176

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:560,495

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1587 SVs from 75 studies. See in: genome view    
    Submitted genomic52,019,050-52,579,544Question Mark
    Overlapping variant regions from other studies: 1587 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):52,885,216-53,445,710Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6722176Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr452,019,05052,579,544
    nsv6722176RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr452,885,21653,445,710

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18691297duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18691297Submitted genomicNC_000004.12:g.520
    19050_52579544dup
    GRCh38 (hg38)NC_000004.12Chr452,019,05052,579,544
    nssv18691297RemappedPerfectNC_000004.11:g.528
    85216_53445710dup
    GRCh37.p13First PassNC_000004.11Chr452,885,21653,445,710

    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)
    nssv186912974e-061275908
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