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nsv6374232

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

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 114 SVs from 19 studies. See in: genome view    
    Submitted genomic139,120,901-139,121,800Question Mark
    Overlapping variant regions from other studies: 114 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):138,839,743-138,840,642Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6374232Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3139,120,901139,121,800
    nsv6374232RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3138,839,743138,840,642

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18093928deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18093928Submitted genomicNC_000003.12:g.139
    120901_139121800de
    l
    GRCh38 (hg38)NC_000003.12Chr3139,120,901139,121,800
    nssv18093928RemappedPerfectNC_000003.11:g.138
    839743_138840642de
    l
    GRCh37.p13First PassNC_000003.11Chr3138,839,743138,840,642

    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)
    nssv18093928<0.001138906
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