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nsv6935031

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20,440

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 213 SVs from 54 studies. See in: genome view    
    Submitted genomic27,934,133-27,954,572Question Mark
    Overlapping variant regions from other studies: 213 SVs from 54 studies. See in: genome view    
    Remapped(Score: Perfect):28,508,270-28,528,709Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6935031Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1327,934,13327,954,572
    nsv6935031RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1328,508,27028,528,709

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18600121duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18600121Submitted genomicNC_000013.11:g.279
    34133_27954572dup
    GRCh38 (hg38)NC_000013.11Chr1327,934,13327,954,572
    nssv18600121RemappedPerfectNC_000013.10:g.285
    08270_28528709dup
    GRCh37.p13First PassNC_000013.10Chr1328,508,27028,528,709

    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)
    nssv186001210.002581275500
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