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nsv6978596

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,960

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 123 SVs from 25 studies. See in: genome view    
    Submitted genomic28,732,597-28,749,556Question Mark
    Overlapping variant regions from other studies: 123 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):27,059,615-27,076,574Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6978596Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1728,732,59728,749,556
    nsv6978596RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1727,059,61527,076,574

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18625693duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18625693Submitted genomicNC_000017.11:g.287
    32597_28749556dup
    GRCh38 (hg38)NC_000017.11Chr1728,732,59728,749,556
    nssv18625693RemappedPerfectNC_000017.10:g.270
    59615_27076574dup
    GRCh37.p13First PassNC_000017.10Chr1727,059,61527,076,574

    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)
    nssv186256931.4e-054271120
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