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nsv6875320

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:23,678

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 267 SVs from 33 studies. See in: genome view    
    Submitted genomic13,390,274-13,413,951Question Mark
    Overlapping variant regions from other studies: 272 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):13,390,273-13,413,950Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6875320Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr913,390,27413,413,951
    nsv6875320RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr913,390,27313,413,950

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18741323duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18741323Submitted genomicNC_000009.12:g.133
    90274_13413951dup
    GRCh38 (hg38)NC_000009.12Chr913,390,27413,413,951
    nssv18741323RemappedPerfectNC_000009.11:g.133
    90273_13413950dup
    GRCh37.p13First PassNC_000009.11Chr913,390,27313,413,950

    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)
    nssv187413234e-061274820
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