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nsv6714641

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:33,283

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 225 SVs from 43 studies. See in: genome view    
    Submitted genomic6,710,403-6,743,685Question Mark
    Overlapping variant regions from other studies: 225 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):6,752,090-6,785,372Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6714641Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr36,710,4036,743,685
    nsv6714641RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr36,752,0906,785,372

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18679959duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18679959Submitted genomicNC_000003.12:g.671
    0403_6743685dup
    GRCh38 (hg38)NC_000003.12Chr36,710,4036,743,685
    nssv18679959RemappedPerfectNC_000003.11:g.675
    2090_6785372dup
    GRCh37.p13First PassNC_000003.11Chr36,752,0906,785,372

    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)
    nssv186799594e-061275396
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