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nsv6936638

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:616

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 81 SVs from 14 studies. See in: genome view    
    Submitted genomic28,147,150-28,147,765Question Mark
    Overlapping variant regions from other studies: 81 SVs from 14 studies. See in: genome view    
    Remapped(Score: Perfect):28,721,287-28,721,902Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6936638Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1328,147,15028,147,765
    nsv6936638RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1328,721,28728,721,902

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18600140duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18600140Submitted genomicNC_000013.11:g.281
    47150_28147765dup
    GRCh38 (hg38)NC_000013.11Chr1328,147,15028,147,765
    nssv18600140RemappedPerfectNC_000013.10:g.287
    21287_28721902dup
    GRCh37.p13First PassNC_000013.10Chr1328,721,28728,721,902

    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)
    nssv186001404e-061246038
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