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nsv6418566

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:804,267

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2023 SVs from 99 studies. See in: genome view    
    Submitted genomic133,866,014-134,670,280Question Mark
    Overlapping variant regions from other studies: 2023 SVs from 99 studies. See in: genome view    
    Remapped(Score: Perfect):134,878,257-135,682,523Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6418566Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8133,866,014134,670,280
    nsv6418566RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8134,878,257135,682,523

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18164702deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18164702Submitted genomicNC_000008.11:g.133
    866014_134670280de
    l
    GRCh38 (hg38)NC_000008.11Chr8133,866,014134,670,280
    nssv18164702RemappedPerfectNC_000008.10:g.134
    878257_135682523de
    l
    GRCh37.p13First PassNC_000008.10Chr8134,878,257135,682,523

    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)
    nssv18164702<0.001223994
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