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nsv6980077

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,657

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 230 SVs from 40 studies. See in: genome view    
    Submitted genomic36,948,522-36,960,178Question Mark
    Overlapping variant regions from other studies: 275 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):35,305,822-35,317,478Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6980077Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1736,948,52236,960,178
    nsv6980077RemappedPerfectGRCh37.p13Primary AssemblySecond PassNC_000017.10Chr1735,305,82235,317,478

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18628617duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18628617Submitted genomicNC_000017.11:g.369
    48522_36960178dup
    GRCh38 (hg38)NC_000017.11Chr1736,948,52236,960,178
    nssv18628617RemappedPerfectNC_000017.10:g.353
    05822_35317478dup
    GRCh37.p13Second PassNC_000017.10Chr1735,305,82235,317,478

    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)
    nssv186286174e-061275762
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