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nsv6571021

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:57

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 117 SVs from 20 studies. See in: genome view    
    Submitted genomic139,114,323-139,114,379Question Mark
    Overlapping variant regions from other studies: 117 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):138,833,165-138,833,221Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6571021Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3139,114,323139,114,379
    nsv6571021RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3138,833,165138,833,221

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18259752inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18259752Submitted genomicNC_000003.12:g.139
    114323_139114379in
    v
    GRCh38 (hg38)NC_000003.12Chr3139,114,323139,114,379
    nssv18259752RemappedPerfectNC_000003.11:g.138
    833165_138833221in
    v
    GRCh37.p13First PassNC_000003.11Chr3138,833,165138,833,221

    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)
    nssv18259752<0.001139304
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