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nsv6400865

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,681

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 30 studies. See in: genome view    
    Submitted genomic140,707,119-140,716,799Question Mark
    Overlapping variant regions from other studies: 112 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):140,086,704-140,096,384Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6400865Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5140,707,119140,716,799
    nsv6400865RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5140,086,704140,096,384

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18215089duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18215089Submitted genomicNC_000005.10:g.140
    707119_140716799du
    p
    GRCh38 (hg38)NC_000005.10Chr5140,707,119140,716,799
    nssv18215089RemappedPerfectNC_000005.9:g.1400
    86704_140096384dup
    GRCh37.p13First PassNC_000005.9Chr5140,086,704140,096,384

    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)
    nssv18215089<0.001439258
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