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nsv6366837

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35,509

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 121 SVs from 30 studies. See in: genome view    
    Submitted genomic48,403,755-48,439,263Question Mark
    Overlapping variant regions from other studies: 121 SVs from 30 studies. See in: genome view    
    Remapped(Score: Good):48,445,162-48,480,673Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6366837Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr348,403,75548,439,263
    nsv6366837RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr348,445,16248,480,673

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18209334duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18209334Submitted genomicNC_000003.12:g.484
    03755_48439263dup
    GRCh38 (hg38)NC_000003.12Chr348,403,75548,439,263
    nssv18209334RemappedGoodNC_000003.11:g.484
    45162_48480673dup
    GRCh37.p13First PassNC_000003.11Chr348,445,16248,480,673

    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)
    nssv18209334<0.001139300
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