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nsv7049242

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,091,676

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4527 SVs from 95 studies. See in: genome view    
    Submitted genomic141,675,999-143,767,674Question Mark
    Overlapping variant regions from other studies: 4527 SVs from 95 studies. See in: genome view    
    Remapped(Score: Perfect):142,433,568-144,525,243Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7049242Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2141,675,999143,767,674
    nsv7049242RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2142,433,568144,525,243

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765859inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765859Submitted genomicNC_000002.12:g.141
    675999_143767674in
    v
    GRCh38 (hg38)NC_000002.12Chr2141,675,999143,767,674
    nssv18765859RemappedPerfectNC_000002.11:g.142
    433568_144525243in
    v
    GRCh37.p13First PassNC_000002.11Chr2142,433,568144,525,243

    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)
    nssv187658594e-061276268
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