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nsv6368234

  • 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: 95 SVs from 24 studies. See in: genome view    
    Submitted genomic87,151,901-87,156,800Question Mark
    Overlapping variant regions from other studies: 95 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):87,201,051-87,205,950Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6368234Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr387,151,90187,156,800
    nsv6368234RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr387,201,05187,205,950

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18104157deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18104157Submitted genomicNC_000003.12:g.871
    51901_87156800del
    GRCh38 (hg38)NC_000003.12Chr387,151,90187,156,800
    nssv18104157RemappedPerfectNC_000003.11:g.872
    01051_87205950del
    GRCh37.p13First PassNC_000003.11Chr387,201,05187,205,950

    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)
    nssv18104157<0.001139094
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