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nsv6486687

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:230,835

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 971 SVs from 73 studies. See in: genome view    
    Submitted genomic122,555,650-122,786,484Question Mark
    Overlapping variant regions from other studies: 971 SVs from 73 studies. See in: genome view    
    Remapped(Score: Perfect):123,040,197-123,271,031Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6486687Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12122,555,650122,786,484
    nsv6486687RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12123,040,197123,271,031

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18183406duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18183406Submitted genomicNC_000012.12:g.122
    555650_122786484du
    p
    GRCh38 (hg38)NC_000012.12Chr12122,555,650122,786,484
    nssv18183406RemappedPerfectNC_000012.11:g.123
    040197_123271031du
    p
    GRCh37.p13First PassNC_000012.11Chr12123,040,197123,271,031

    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)
    nssv18183406<0.001139220
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