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nsv6882110

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:158

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 112 SVs from 17 studies. See in: genome view    
    Submitted genomic123,143,489-123,143,646Question Mark
    Overlapping variant regions from other studies: 112 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):124,903,005-124,903,162Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6882110Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10123,143,489123,143,646
    nsv6882110RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10124,903,005124,903,162

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18571275duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18571275Submitted genomicNC_000010.11:g.123
    143489_123143646du
    p
    GRCh38 (hg38)NC_000010.11Chr10123,143,489123,143,646
    nssv18571275RemappedPerfectNC_000010.10:g.124
    903005_124903162du
    p
    GRCh37.p13First PassNC_000010.10Chr10124,903,005124,903,162

    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)
    nssv185712752.1e-055230618
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