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nsv6860019

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:219,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 941 SVs from 74 studies. See in: genome view    
    Submitted genomic128,721,801-128,940,900Question Mark
    Overlapping variant regions from other studies: 941 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):131,484,080-131,703,179Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6860019Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9128,721,801128,940,900
    nsv6860019RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9131,484,080131,703,179

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18732970duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18732970Submitted genomicNC_000009.12:g.128
    721801_128940900du
    p
    GRCh38 (hg38)NC_000009.12Chr9128,721,801128,940,900
    nssv18732970RemappedPerfectNC_000009.11:g.131
    484080_131703179du
    p
    GRCh37.p13First PassNC_000009.11Chr9131,484,080131,703,179

    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)
    nssv187329704e-061275402
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