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nsv6375470

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,562

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 92 SVs from 18 studies. See in: genome view    
    Submitted genomic179,618,883-179,620,444Question Mark
    Overlapping variant regions from other studies: 92 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):179,336,671-179,338,232Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6375470Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3179,618,883179,620,444
    nsv6375470RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3179,336,671179,338,232

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18211519duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18211519Submitted genomicNC_000003.12:g.179
    618883_179620444du
    p
    GRCh38 (hg38)NC_000003.12Chr3179,618,883179,620,444
    nssv18211519RemappedPerfectNC_000003.11:g.179
    336671_179338232du
    p
    GRCh37.p13First PassNC_000003.11Chr3179,336,671179,338,232

    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)
    nssv18211519<0.001238756
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