nsv6676857

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:183

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 131 SVs from 23 studies. See in: genome view    
    Submitted genomic229,453,222-229,453,404Question Mark
    Overlapping variant regions from other studies: 134 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):229,588,969-229,589,151Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6676857Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1229,453,222229,453,404
    nsv6676857RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1229,588,969229,589,151

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18609463duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18609463Submitted genomicNC_000001.11:g.229
    453222_229453404du
    p
    GRCh38 (hg38)NC_000001.11Chr1229,453,222229,453,404
    nssv18609463RemappedPerfectNC_000001.10:g.229
    588969_229589151du
    p
    GRCh37.p13First PassNC_000001.10Chr1229,588,969229,589,151

    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)
    nssv186094630.04510044230044
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