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nsv6723076

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:280

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 123 SVs from 33 studies. See in: genome view    
    Submitted genomic57,431,189-57,431,468Question Mark
    Overlapping variant regions from other studies: 123 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):58,297,355-58,297,634Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6723076Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr457,431,18957,431,468
    nsv6723076RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr458,297,35558,297,634

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18691661duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18691661Submitted genomicNC_000004.12:g.574
    31189_57431468dup
    GRCh38 (hg38)NC_000004.12Chr457,431,18957,431,468
    nssv18691661RemappedPerfectNC_000004.11:g.582
    97355_58297634dup
    GRCh37.p13First PassNC_000004.11Chr458,297,35558,297,634

    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)
    nssv186916618e-062232708
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