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nsv6469930

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:56,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 248 SVs from 54 studies. See in: genome view    
    Submitted genomic55,367,501-55,424,000Question Mark
    Overlapping variant regions from other studies: 248 SVs from 54 studies. See in: genome view    
    Remapped(Score: Perfect):55,761,285-55,817,784Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6469930Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1255,367,50155,424,000
    nsv6469930RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1255,761,28555,817,784

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18183845duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18183845Submitted genomicNC_000012.12:g.553
    67501_55424000dup
    GRCh38 (hg38)NC_000012.12Chr1255,367,50155,424,000
    nssv18183845RemappedPerfectNC_000012.11:g.557
    61285_55817784dup
    GRCh37.p13First PassNC_000012.11Chr1255,761,28555,817,784

    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)
    nssv18183845<0.001138730
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