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nsv6499605

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20,327

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 279 SVs from 50 studies. See in: genome view    
    Submitted genomic41,093,195-41,113,521Question Mark
    Overlapping variant regions from other studies: 277 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):39,249,447-39,269,773Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6499605Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1741,093,19541,113,521
    nsv6499605RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1739,249,44739,269,773

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18189137duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18189137Submitted genomicNC_000017.11:g.410
    93195_41113521dup
    GRCh38 (hg38)NC_000017.11Chr1741,093,19541,113,521
    nssv18189137RemappedPerfectNC_000017.10:g.392
    49447_39269773dup
    GRCh37.p13First PassNC_000017.10Chr1739,249,44739,269,773

    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)
    nssv18189137<0.001238732
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