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nsv6772768

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:357,253

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 962 SVs from 71 studies. See in: genome view    
    Submitted genomic58,136,555-58,493,807Question Mark
    Overlapping variant regions from other studies: 962 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):57,432,382-57,789,634Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6772768Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr558,136,55558,493,807
    nsv6772768RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr557,432,38257,789,634

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18705382duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18705382Submitted genomicNC_000005.10:g.581
    36555_58493807dup
    GRCh38 (hg38)NC_000005.10Chr558,136,55558,493,807
    nssv18705382RemappedPerfectNC_000005.9:g.5743
    2382_57789634dup
    GRCh37.p13First PassNC_000005.9Chr557,432,38257,789,634

    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)
    nssv187053824e-061275362
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