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nsv6673170

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:233,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1148 SVs from 74 studies. See in: genome view    
    Submitted genomic3,418,301-3,651,400Question Mark
    Overlapping variant regions from other studies: 1121 SVs from 74 studies. See in: genome view    
    Remapped(Score: Pass):3,422,072-3,698,990Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6673170Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr23,418,3013,651,400
    nsv6673170RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr23,422,0723,698,990

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18663163duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18663163Submitted genomicNC_000002.12:g.341
    8301_3651400dup
    GRCh38 (hg38)NC_000002.12Chr23,418,3013,651,400
    nssv18663163RemappedPassNC_000002.11:g.342
    2072_3698990dup
    GRCh37.p13First PassNC_000002.11Chr23,422,0723,698,990

    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)
    nssv186631637.8e-0521263204
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