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nsv6987699

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20,692

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 160 SVs from 33 studies. See in: genome view    
    Submitted genomic67,178,586-67,199,277Question Mark
    Overlapping variant regions from other studies: 160 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):67,212,489-67,233,180Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6987699Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1667,178,58667,199,277
    nsv6987699RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1667,212,48967,233,180

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18623687duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18623687Submitted genomicNC_000016.10:g.671
    78586_67199277dup
    GRCh38 (hg38)NC_000016.10Chr1667,178,58667,199,277
    nssv18623687RemappedPerfectNC_000016.9:g.6721
    2489_67233180dup
    GRCh37.p13First PassNC_000016.9Chr1667,212,48967,233,180

    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)
    nssv186236874e-061275382
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