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nsv6986046

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:863,075

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2709 SVs from 85 studies. See in: genome view    
    Submitted genomic73,831,787-74,694,861Question Mark
    Overlapping variant regions from other studies: 2709 SVs from 85 studies. See in: genome view    
    Remapped(Score: Perfect):71,827,926-72,691,000Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6986046Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1773,831,78774,694,861
    nsv6986046RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1771,827,92672,691,000

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18628892duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18628892Submitted genomicNC_000017.11:g.738
    31787_74694861dup
    GRCh38 (hg38)NC_000017.11Chr1773,831,78774,694,861
    nssv18628892RemappedPerfectNC_000017.10:g.718
    27926_72691000dup
    GRCh37.p13First PassNC_000017.10Chr1771,827,92672,691,000

    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)
    nssv18628892<0.001167274560
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