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nsv6930590

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:407,245

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1398 SVs from 81 studies. See in: genome view    
    Submitted genomic8,482,988-8,890,232Question Mark
    Overlapping variant regions from other studies: 1398 SVs from 81 studies. See in: genome view    
    Remapped(Score: Perfect):8,635,584-9,042,828Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6930590Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr128,482,9888,890,232
    nsv6930590RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr128,635,5849,042,828

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18600282duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18600282Submitted genomicNC_000012.12:g.848
    2988_8890232dup
    GRCh38 (hg38)NC_000012.12Chr128,482,9888,890,232
    nssv18600282RemappedPerfectNC_000012.11:g.863
    5584_9042828dup
    GRCh37.p13First PassNC_000012.11Chr128,635,5849,042,828

    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)
    nssv186002824e-061275884
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