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nsv6865244

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:112,687

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 442 SVs from 55 studies. See in: genome view    
    Submitted genomic21,423,859-21,536,545Question Mark
    Overlapping variant regions from other studies: 448 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):21,423,858-21,536,544Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6865244Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr921,423,85921,536,545
    nsv6865244RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr921,423,85821,536,544

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18565947deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18565947Submitted genomicNC_000009.12:g.214
    23859_21536545del
    GRCh38 (hg38)NC_000009.12Chr921,423,85921,536,545
    nssv18565947RemappedPerfectNC_000009.11:g.214
    23858_21536544del
    GRCh37.p13First PassNC_000009.11Chr921,423,85821,536,544

    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)
    nssv185659474e-061276110
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