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nsv6983143

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:83,480

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 370 SVs from 39 studies. See in: genome view    
    Submitted genomic50,751,981-50,835,460Question Mark
    Overlapping variant regions from other studies: 369 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):48,829,342-48,912,821Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6983143Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1750,751,98150,835,460
    nsv6983143RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1748,829,34248,912,821

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18626705duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18626705Submitted genomicNC_000017.11:g.507
    51981_50835460dup
    GRCh38 (hg38)NC_000017.11Chr1750,751,98150,835,460
    nssv18626705RemappedPerfectNC_000017.10:g.488
    29342_48912821dup
    GRCh37.p13First PassNC_000017.10Chr1748,829,34248,912,821

    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)
    nssv186267054e-061273176
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