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nsv6547571

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,937

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 169 SVs from 21 studies. See in: genome view    
    Submitted genomic39,178,912-39,180,848Question Mark
    Overlapping variant regions from other studies: 169 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):40,550,838-40,552,774Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6547571Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2139,178,91239,180,848
    nsv6547571RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2140,550,83840,552,774

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18072381deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18072381Submitted genomicNC_000021.9:g.3917
    8912_39180848del
    GRCh38 (hg38)NC_000021.9Chr2139,178,91239,180,848
    nssv18072381RemappedPerfectNC_000021.8:g.4055
    0838_40552774del
    GRCh37.p13First PassNC_000021.8Chr2140,550,83840,552,774

    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)
    nssv18072381<0.001138998
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