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nsv6869503

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 147 SVs from 31 studies. See in: genome view    
    Submitted genomic133,032,101-133,037,800Question Mark
    Overlapping variant regions from other studies: 147 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):135,907,488-135,913,187Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6869503Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9133,032,101133,037,800
    nsv6869503RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9135,907,488135,913,187

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18565114deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18565114Submitted genomicNC_000009.12:g.133
    032101_133037800de
    l
    GRCh38 (hg38)NC_000009.12Chr9133,032,101133,037,800
    nssv18565114RemappedPerfectNC_000009.11:g.135
    907488_135913187de
    l
    GRCh37.p13First PassNC_000009.11Chr9135,907,488135,913,187

    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)
    nssv18565114<0.001237252704
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