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nsv6554443

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,647

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 173 SVs from 24 studies. See in: genome view    
    Submitted genomic38,817,456-38,819,102Question Mark
    Overlapping variant regions from other studies: 173 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):40,189,380-40,191,026Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6554443Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2138,817,45638,819,102
    nsv6554443RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2140,189,38040,191,026

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18072362deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18072362Submitted genomicNC_000021.9:g.3881
    7456_38819102del
    GRCh38 (hg38)NC_000021.9Chr2138,817,45638,819,102
    nssv18072362RemappedPerfectNC_000021.8:g.4018
    9380_40191026del
    GRCh37.p13First PassNC_000021.8Chr2140,189,38040,191,026

    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)
    nssv18072362<0.001338922
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