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nsv6318284

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:704

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 23 studies. See in: genome view    
    Submitted genomic159,427,297-159,428,000Question Mark
    Overlapping variant regions from other studies: 115 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):159,397,087-159,397,790Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6318284Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1159,427,297159,428,000
    nsv6318284RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1159,397,087159,397,790

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18053525deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18053525Submitted genomicNC_000001.11:g.159
    427297_159428000de
    l
    GRCh38 (hg38)NC_000001.11Chr1159,427,297159,428,000
    nssv18053525RemappedPerfectNC_000001.10:g.159
    397087_159397790de
    l
    GRCh37.p13First PassNC_000001.10Chr1159,397,087159,397,790

    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)
    nssv18053525<0.001338186
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