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nsv6847992

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:623,935

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1322 SVs from 74 studies. See in: genome view    
    Submitted genomic54,863,026-55,486,960Question Mark
    Overlapping variant regions from other studies: 1322 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):55,775,586-56,399,520Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6847992Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr854,863,02655,486,960
    nsv6847992RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr855,775,58656,399,520

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18732493duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18732493Submitted genomicNC_000008.11:g.548
    63026_55486960dup
    GRCh38 (hg38)NC_000008.11Chr854,863,02655,486,960
    nssv18732493RemappedPerfectNC_000008.10:g.557
    75586_56399520dup
    GRCh37.p13First PassNC_000008.10Chr855,775,58656,399,520

    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)
    nssv187324934e-061275572
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