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nsv7061212

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,304

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 246 SVs from 28 studies. See in: genome view    
    Submitted genomic113,493,054-113,496,357Question Mark
    Overlapping variant regions from other studies: 249 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):114,147,369-114,150,672Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7061212Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr13113,493,054113,496,357
    nsv7061212RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr13114,147,369114,150,672

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18752165inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18752165Submitted genomicNC_000013.11:g.113
    493054_113496357in
    v
    GRCh38 (hg38)NC_000013.11Chr13113,493,054113,496,357
    nssv18752165RemappedPerfectNC_000013.10:g.114
    147369_114150672in
    v
    GRCh37.p13First PassNC_000013.10Chr13114,147,369114,150,672

    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)
    nssv187521654e-061276268
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