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nsv6679072

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:549,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1641 SVs from 79 studies. See in: genome view    
    Submitted genomic233,093,901-233,643,200Question Mark
    Overlapping variant regions from other studies: 1614 SVs from 80 studies. See in: genome view    
    Remapped(Score: Pass):233,958,611-234,551,846Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6679072Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2233,093,901233,643,200
    nsv6679072RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2233,958,611234,551,846

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18450334deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18450334Submitted genomicNC_000002.12:g.233
    093901_233643200de
    l
    GRCh38 (hg38)NC_000002.12Chr2233,093,901233,643,200
    nssv18450334RemappedPassNC_000002.11:g.233
    958611_234551846de
    l
    GRCh37.p13First PassNC_000002.11Chr2233,958,611234,551,846

    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)
    nssv184503344e-061276238
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