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nsv6319663

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,702

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 167 SVs from 40 studies. See in: genome view    
    Submitted genomic92,211,704-92,216,405Question Mark
    Overlapping variant regions from other studies: 167 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):92,677,261-92,681,962Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6319663Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr192,211,70492,216,405
    nsv6319663RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr192,677,26192,681,962

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18065172deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18065172Submitted genomicNC_000001.11:g.922
    11704_92216405del
    GRCh38 (hg38)NC_000001.11Chr192,211,70492,216,405
    nssv18065172RemappedPerfectNC_000001.10:g.926
    77261_92681962del
    GRCh37.p13First PassNC_000001.10Chr192,677,26192,681,962

    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)
    nssv18065172<0.001139238
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