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nsv6692919

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:71,541

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 280 SVs from 50 studies. See in: genome view    
    Submitted genomic228,485,236-228,556,776Question Mark
    Overlapping variant regions from other studies: 280 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):229,349,952-229,421,492Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6692919Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2228,485,236228,556,776
    nsv6692919RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2229,349,952229,421,492

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18450238deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18450238Submitted genomicNC_000002.12:g.228
    485236_228556776de
    l
    GRCh38 (hg38)NC_000002.12Chr2228,485,236228,556,776
    nssv18450238RemappedPerfectNC_000002.11:g.229
    349952_229421492de
    l
    GRCh37.p13First PassNC_000002.11Chr2229,349,952229,421,492

    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)
    nssv184502383.9e-052275354
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