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nsv7044064

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,984,887

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 18583 SVs from 123 studies. See in: genome view    
    Submitted genomic112,019,946-120,004,832Question Mark
    Overlapping variant regions from other studies: 18591 SVs from 123 studies. See in: genome view    
    Remapped(Score: Perfect):112,777,523-120,762,408Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044064Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2112,019,946120,004,832
    nsv7044064RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2112,777,523120,762,408

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767527inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767527Submitted genomicNC_000002.12:g.112
    019946_120004832in
    v
    GRCh38 (hg38)NC_000002.12Chr2112,019,946120,004,832
    nssv18767527RemappedPerfectNC_000002.11:g.112
    777523_120762408in
    v
    GRCh37.p13First PassNC_000002.11Chr2112,777,523120,762,408

    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)
    nssv187675274e-061276262
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