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nsv6481464

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:802

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 82 SVs from 23 studies. See in: genome view    
    Submitted genomic70,654,450-70,655,251Question Mark
    Overlapping variant regions from other studies: 82 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):71,121,167-71,121,968Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6481464Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1470,654,45070,655,251
    nsv6481464RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1471,121,16771,121,968

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18187081duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18187081Submitted genomicNC_000014.9:g.7065
    4450_70655251dup
    GRCh38 (hg38)NC_000014.9Chr1470,654,45070,655,251
    nssv18187081RemappedPerfectNC_000014.8:g.7112
    1167_71121968dup
    GRCh37.p13First PassNC_000014.8Chr1471,121,16771,121,968

    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)
    nssv18187081<0.0011038682
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