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nsv6472196

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,070,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3949 SVs from 102 studies. See in: genome view    
    Submitted genomic6,013,501-7,083,700Question Mark
    Overlapping variant regions from other studies: 3928 SVs from 102 studies. See in: genome view    
    Remapped(Score: Good):6,122,667-7,189,876Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6472196Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr126,013,5017,083,700
    nsv6472196RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr126,122,6677,189,876

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18178682duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18178682Submitted genomicNC_000012.12:g.601
    3501_7083700dup
    GRCh38 (hg38)NC_000012.12Chr126,013,5017,083,700
    nssv18178682RemappedGoodNC_000012.11:g.612
    2667_7189876dup
    GRCh37.p13First PassNC_000012.11Chr126,122,6677,189,876

    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)
    nssv18178682<0.0012339146
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