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nsv6453323

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:158,975

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 392 SVs from 55 studies. See in: genome view    
    Submitted genomic32,747,382-32,906,356Question Mark
    Overlapping variant regions from other studies: 392 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):33,036,310-33,195,284Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6453323Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1032,747,38232,906,356
    nsv6453323RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1033,036,31033,195,284

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18183993duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18183993Submitted genomicNC_000010.11:g.327
    47382_32906356dup
    GRCh38 (hg38)NC_000010.11Chr1032,747,38232,906,356
    nssv18183993RemappedPerfectNC_000010.10:g.330
    36310_33195284dup
    GRCh37.p13First PassNC_000010.10Chr1033,036,31033,195,284

    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)
    nssv18183993<0.001139254
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