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nsv6604708

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:778,639

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3501 SVs from 110 studies. See in: genome view    
    Submitted genomic100,460,230-101,238,868Question Mark
    Overlapping variant regions from other studies: 3440 SVs from 110 studies. See in: genome view    
    Remapped(Score: Pass):100,057,853-100,882,149Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6604708Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7100,460,230101,238,868
    nsv6604708RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7100,057,853100,882,149

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18222599duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18222599Submitted genomicNC_000007.14:g.100
    460230_101238868du
    p
    GRCh38 (hg38)NC_000007.14Chr7100,460,230101,238,868
    nssv18222599RemappedPassNC_000007.13:g.100
    057853_100882149du
    p
    GRCh37.p13First PassNC_000007.13Chr7100,057,853100,882,149

    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)
    nssv18222599<0.001138694
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