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nsv6776040

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,754

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 121 SVs from 27 studies. See in: genome view    
    Submitted genomic31,888,435-31,892,188Question Mark
    Overlapping variant regions from other studies: 121 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):31,888,541-31,892,294Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6776040Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr531,888,43531,892,188
    nsv6776040RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr531,888,54131,892,294

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18703464duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18703464Submitted genomicNC_000005.10:g.318
    88435_31892188dup
    GRCh38 (hg38)NC_000005.10Chr531,888,43531,892,188
    nssv18703464RemappedPerfectNC_000005.9:g.3188
    8541_31892294dup
    GRCh37.p13First PassNC_000005.9Chr531,888,54131,892,294

    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)
    nssv187034644e-061275218
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