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nsv6382663

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,780

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 185 SVs from 32 studies. See in: genome view    
    Submitted genomic165,090,188-165,094,967Question Mark
    Overlapping variant regions from other studies: 185 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):166,011,340-166,016,119Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6382663Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4165,090,188165,094,967
    nsv6382663RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4166,011,340166,016,119

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18213805duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18213805Submitted genomicNC_000004.12:g.165
    090188_165094967du
    p
    GRCh38 (hg38)NC_000004.12Chr4165,090,188165,094,967
    nssv18213805RemappedPerfectNC_000004.11:g.166
    011340_166016119du
    p
    GRCh37.p13First PassNC_000004.11Chr4166,011,340166,016,119

    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)
    nssv18213805<0.001139270
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