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nsv7024455

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 205 SVs from 38 studies. See in: genome view    
    Submitted genomic39,418,601-39,423,500Question Mark
    Overlapping variant regions from other studies: 205 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):40,790,527-40,795,426Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7024455Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2139,418,60139,423,500
    nsv7024455RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2140,790,52740,795,426

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18436364deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18436364Submitted genomicNC_000021.9:g.3941
    8601_39423500del
    GRCh38 (hg38)NC_000021.9Chr2139,418,60139,423,500
    nssv18436364RemappedPerfectNC_000021.8:g.4079
    0527_40795426del
    GRCh37.p13First PassNC_000021.8Chr2140,790,52740,795,426

    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)
    nssv184363644e-061275942
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