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nsv6885385

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 490 SVs from 55 studies. See in: genome view    
    Submitted genomic137,048,801-137,056,400Question Mark
    Overlapping variant regions from other studies: 490 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):139,943,253-139,950,852Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6885385Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9137,048,801137,056,400
    nsv6885385RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9139,943,253139,950,852

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18737639duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18737639Submitted genomicNC_000009.12:g.137
    048801_137056400du
    p
    GRCh38 (hg38)NC_000009.12Chr9137,048,801137,056,400
    nssv18737639RemappedPerfectNC_000009.11:g.139
    943253_139950852du
    p
    GRCh37.p13First PassNC_000009.11Chr9139,943,253139,950,852

    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)
    nssv187376394e-061238390
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