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nsv6747792

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:103,687

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 437 SVs from 43 studies. See in: genome view    
    Submitted genomic86,845,822-86,949,508Question Mark
    Overlapping variant regions from other studies: 437 SVs from 43 studies. See in: genome view    
    Remapped(Score: Good):87,766,975-87,870,660Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6747792Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr486,845,82286,949,508
    nsv6747792RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr487,766,97587,870,660

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18691468duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18691468Submitted genomicNC_000004.12:g.868
    45822_86949508dup
    GRCh38 (hg38)NC_000004.12Chr486,845,82286,949,508
    nssv18691468RemappedGoodNC_000004.11:g.877
    66975_87870660dup
    GRCh37.p13First PassNC_000004.11Chr487,766,97587,870,660

    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)
    nssv186914684e-061275704
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