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nsv6927748

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:27,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 410 SVs from 58 studies. See in: genome view    
    Submitted genomic132,670,201-132,697,600Question Mark
    Overlapping variant regions from other studies: 410 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):133,246,787-133,274,186Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6927748Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12132,670,201132,697,600
    nsv6927748RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12133,246,787133,274,186

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18595573duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18595573Submitted genomicNC_000012.12:g.132
    670201_132697600du
    p
    GRCh38 (hg38)NC_000012.12Chr12132,670,201132,697,600
    nssv18595573RemappedPerfectNC_000012.11:g.133
    246787_133274186du
    p
    GRCh37.p13First PassNC_000012.11Chr12133,246,787133,274,186

    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)
    nssv185955731.4e-054275732
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