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nsv7054651

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,922

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 157 SVs from 30 studies. See in: genome view    
    Submitted genomic112,290,713-112,297,634Question Mark
    Overlapping variant regions from other studies: 157 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):111,626,410-111,633,331Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7054651Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5112,290,713112,297,634
    nsv7054651RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5111,626,410111,633,331

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18774440inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18774440Submitted genomicNC_000005.10:g.112
    290713_112297634in
    v
    GRCh38 (hg38)NC_000005.10Chr5112,290,713112,297,634
    nssv18774440RemappedPerfectNC_000005.9:g.1116
    26410_111633331inv
    GRCh37.p13First PassNC_000005.9Chr5111,626,410111,633,331

    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)
    nssv187744404e-060276268
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