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nsv6697501

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 91 SVs from 20 studies. See in: genome view    
    Submitted genomic74,628,601-74,630,900Question Mark
    Overlapping variant regions from other studies: 91 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):74,855,728-74,858,027Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6697501Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr274,628,60174,630,900
    nsv6697501RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr274,855,72874,858,027

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18666871duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18666871Submitted genomicNC_000002.12:g.746
    28601_74630900dup
    GRCh38 (hg38)NC_000002.12Chr274,628,60174,630,900
    nssv18666871RemappedPerfectNC_000002.11:g.748
    55728_74858027dup
    GRCh37.p13First PassNC_000002.11Chr274,855,72874,858,027

    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)
    nssv186668717.6e-0521268640
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