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nsv6647879

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,014,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4450 SVs from 104 studies. See in: genome view    
    Submitted genomic2,800,201-3,815,100Question Mark
    Overlapping variant regions from other studies: 4450 SVs from 104 studies. See in: genome view    
    Remapped(Score: Perfect):2,716,766-3,731,664Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6647879Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr12,800,2013,815,100
    nsv6647879RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr12,716,7663,731,664

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18608074duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18608074Submitted genomicNC_000001.11:g.280
    0201_3815100dup
    GRCh38 (hg38)NC_000001.11Chr12,800,2013,815,100
    nssv18608074RemappedPerfectNC_000001.10:g.271
    6766_3731664dup
    GRCh37.p13First PassNC_000001.10Chr12,716,7663,731,664

    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)
    nssv186080744e-061269410
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