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nsv6472373

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,071,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3938 SVs from 102 studies. See in: genome view    
    Submitted genomic6,012,501-7,083,600Question Mark
    Overlapping variant regions from other studies: 3929 SVs from 102 studies. See in: genome view    
    Remapped(Score: Good):6,121,667-7,189,876Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6472373Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr126,012,5017,083,600
    nsv6472373RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr126,121,6677,189,876

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18189116duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18189116Submitted genomicNC_000012.12:g.601
    2501_7083600dup
    GRCh38 (hg38)NC_000012.12Chr126,012,5017,083,600
    nssv18189116RemappedGoodNC_000012.11:g.612
    1667_7189876dup
    GRCh37.p13First PassNC_000012.11Chr126,121,6677,189,876

    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)
    nssv18189116<0.0012339096
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