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nsv6691520

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:198,291

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 512 SVs from 72 studies. See in: genome view    
    Submitted genomic150,460,419-150,658,709Question Mark
    Overlapping variant regions from other studies: 512 SVs from 72 studies. See in: genome view    
    Remapped(Score: Perfect):151,316,933-151,515,223Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6691520Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2150,460,419150,658,709
    nsv6691520RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2151,316,933151,515,223

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18647876duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18647876Submitted genomicNC_000002.12:g.150
    460419_150658709du
    p
    GRCh38 (hg38)NC_000002.12Chr2150,460,419150,658,709
    nssv18647876RemappedPerfectNC_000002.11:g.151
    316933_151515223du
    p
    GRCh37.p13First PassNC_000002.11Chr2151,316,933151,515,223

    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)
    nssv186478764e-061275458
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