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nsv7077669

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:79,188

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 349 SVs from 47 studies. See in: genome view    
    Submitted genomic117,124,022-117,203,209Question Mark
    Overlapping variant regions from other studies: 349 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):116,994,738-117,073,925Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077669Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11117,124,022117,203,209
    nsv7077669RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11116,994,738117,073,925

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18747127inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18747127Submitted genomicNC_000011.10:g.117
    124022_117203209in
    v
    GRCh38 (hg38)NC_000011.10Chr11117,124,022117,203,209
    nssv18747127RemappedPerfectNC_000011.9:g.1169
    94738_117073925inv
    GRCh37.p13First PassNC_000011.9Chr11116,994,738117,073,925

    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)
    nssv187471274e-061276268
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