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nsv6690684

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,981

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 85 SVs from 20 studies. See in: genome view    
    Submitted genomic228,011,802-228,014,782Question Mark
    Overlapping variant regions from other studies: 85 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):228,876,518-228,879,498Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6690684Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2228,011,802228,014,782
    nsv6690684RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2228,876,518228,879,498

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18450233deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18450233Submitted genomicNC_000002.12:g.228
    011802_228014782de
    l
    GRCh38 (hg38)NC_000002.12Chr2228,011,802228,014,782
    nssv18450233RemappedPerfectNC_000002.11:g.228
    876518_228879498de
    l
    GRCh37.p13First PassNC_000002.11Chr2228,876,518228,879,498

    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)
    nssv184502334e-061276054
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