nsv7056039

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,936

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 137 SVs from 25 studies. See in: genome view    
    Submitted genomic133,573,259-133,578,194Question Mark
    Overlapping variant regions from other studies: 137 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):134,330,830-134,335,765Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7056039Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2133,573,259133,578,194
    nsv7056039RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2134,330,830134,335,765

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765746inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765746Submitted genomicNC_000002.12:g.133
    573259_133578194in
    v
    GRCh38 (hg38)NC_000002.12Chr2133,573,259133,578,194
    nssv18765746RemappedPerfectNC_000002.11:g.134
    330830_134335765in
    v
    GRCh37.p13First PassNC_000002.11Chr2134,330,830134,335,765

    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)
    nssv187657466.8e-052275036
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