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nsv6340879

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 135 SVs from 20 studies. See in: genome view    
    Submitted genomic186,703,801-186,704,600Question Mark
    Overlapping variant regions from other studies: 135 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):187,568,528-187,569,327Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6340879Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2186,703,801186,704,600
    nsv6340879RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2187,568,528187,569,327

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18080695deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18080695Submitted genomicNC_000002.12:g.186
    703801_186704600de
    l
    GRCh38 (hg38)NC_000002.12Chr2186,703,801186,704,600
    nssv18080695RemappedPerfectNC_000002.11:g.187
    568528_187569327de
    l
    GRCh37.p13First PassNC_000002.11Chr2187,568,528187,569,327

    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)
    nssv18080695<0.001338650
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