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nsv6736543

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:165,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 619 SVs from 59 studies. See in: genome view    
    Submitted genomic194,217,201-194,382,500Question Mark
    Overlapping variant regions from other studies: 596 SVs from 59 studies. See in: genome view    
    Remapped(Score: Good):193,934,990-194,103,229Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6736543Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3194,217,201194,382,500
    nsv6736543RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3193,934,990194,103,229

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18676638duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18676638Submitted genomicNC_000003.12:g.194
    217201_194382500du
    p
    GRCh38 (hg38)NC_000003.12Chr3194,217,201194,382,500
    nssv18676638RemappedGoodNC_000003.11:g.193
    934990_194103229du
    p
    GRCh37.p13First PassNC_000003.11Chr3193,934,990194,103,229

    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)
    nssv186766384.4e-059199956
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