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nsv6317466

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,130

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 136 SVs from 34 studies. See in: genome view    
    Submitted genomic119,824,668-119,831,797Question Mark
    Overlapping variant regions from other studies: 138 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):120,367,291-120,374,420Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6317466Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1119,824,668119,831,797
    nsv6317466RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1120,367,291120,374,420

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18051284deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18051284Submitted genomicNC_000001.11:g.119
    824668_119831797de
    l
    GRCh38 (hg38)NC_000001.11Chr1119,824,668119,831,797
    nssv18051284RemappedPerfectNC_000001.10:g.120
    367291_120374420de
    l
    GRCh37.p13First PassNC_000001.10Chr1120,367,291120,374,420

    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)
    nssv18051284<0.001239270
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