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nsv6551420

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:805,755

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5957 SVs from 120 studies. See in: genome view    
    Submitted genomic22,099,252-22,905,006Question Mark
    Overlapping variant regions from other studies: 5998 SVs from 120 studies. See in: genome view    
    Remapped(Score: Good):22,453,662-23,247,186Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6551420Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2222,099,25222,905,006
    nsv6551420RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2222,453,66223,247,186

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18072628deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18072628Submitted genomicNC_000022.11:g.220
    99252_22905006del
    GRCh38 (hg38)NC_000022.11Chr2222,099,25222,905,006
    nssv18072628RemappedGoodNC_000022.10:g.224
    53662_23247186del
    GRCh37.p13First PassNC_000022.10Chr2222,453,66223,247,186

    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)
    nssv18072628<0.001138990
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