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nsv6726366

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:73,641

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 447 SVs from 73 studies. See in: genome view    
    Submitted genomic184,370,553-184,444,193Question Mark
    Overlapping variant regions from other studies: 447 SVs from 73 studies. See in: genome view    
    Remapped(Score: Perfect):184,088,341-184,161,981Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6726366Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3184,370,553184,444,193
    nsv6726366RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3184,088,341184,161,981

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18477919deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18477919Submitted genomicNC_000003.12:g.184
    370553_184444193de
    l
    GRCh38 (hg38)NC_000003.12Chr3184,370,553184,444,193
    nssv18477919RemappedPerfectNC_000003.11:g.184
    088341_184161981de
    l
    GRCh37.p13First PassNC_000003.11Chr3184,088,341184,161,981

    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)
    nssv184779194e-061275980
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