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nsv6925230

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:484,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1805 SVs from 86 studies. See in: genome view    
    Submitted genomic6,418,401-6,902,400Question Mark
    Overlapping variant regions from other studies: 1392 SVs from 85 studies. See in: genome view    
    Remapped(Score: Pass):6,527,567-6,907,580Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6925230Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr126,418,4016,902,400
    nsv6925230RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr126,527,5676,907,580

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18597050duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18597050Submitted genomicNC_000012.12:g.641
    8401_6902400dup
    GRCh38 (hg38)NC_000012.12Chr126,418,4016,902,400
    nssv18597050RemappedPassNC_000012.11:g.652
    7567_6907580dup
    GRCh37.p13First PassNC_000012.11Chr126,527,5676,907,580

    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)
    nssv185970507.3e-0520268720
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