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nsv6839804

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:368

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 141 SVs from 14 studies. See in: genome view    
    Submitted genomic101,983,143-101,983,510Question Mark
    Overlapping variant regions from other studies: 141 SVs from 14 studies. See in: genome view    
    Remapped(Score: Perfect):102,995,371-102,995,738Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6839804Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8101,983,143101,983,510
    nsv6839804RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8102,995,371102,995,738

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18729980duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18729980Submitted genomicNC_000008.11:g.101
    983143_101983510du
    p
    GRCh38 (hg38)NC_000008.11Chr8101,983,143101,983,510
    nssv18729980RemappedPerfectNC_000008.10:g.102
    995371_102995738du
    p
    GRCh37.p13First PassNC_000008.10Chr8102,995,371102,995,738

    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)
    nssv187299804e-061242578
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