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nsv6987531

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 212 SVs from 40 studies. See in: genome view    
    Submitted genomic19,044,801-19,070,000Question Mark
    Overlapping variant regions from other studies: 212 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):19,056,123-19,081,322Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6987531Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1619,044,80119,070,000
    nsv6987531RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1619,056,12319,081,322

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18619983duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18619983Submitted genomicNC_000016.10:g.190
    44801_19070000dup
    GRCh38 (hg38)NC_000016.10Chr1619,044,80119,070,000
    nssv18619983RemappedPerfectNC_000016.9:g.1905
    6123_19081322dup
    GRCh37.p13First PassNC_000016.9Chr1619,056,12319,081,322

    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)
    nssv186199837e-062276084
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