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nsv7066153

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:954,623

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7065 SVs from 104 studies. See in: genome view    
    Submitted genomic113,377,803-114,332,425Question Mark
    Overlapping variant regions from other studies: 6917 SVs from 104 studies. See in: genome view    
    Remapped(Score: Pass):114,032,118-115,085,141Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066153Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr13113,377,803114,332,425
    nsv7066153RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr13114,032,118115,085,141

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18752162inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18752162Submitted genomicNC_000013.11:g.113
    377803_114332425in
    v
    GRCh38 (hg38)NC_000013.11Chr13113,377,803114,332,425
    nssv18752162RemappedPassNC_000013.10:g.114
    032118_115085141in
    v
    GRCh37.p13First PassNC_000013.10Chr13114,032,118115,085,141

    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)
    nssv187521624e-061276264
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