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nsv6797723

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:29,465

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 240 SVs from 48 studies. See in: genome view    
    Submitted genomic31,087,810-31,117,274Question Mark
    Overlapping variant regions from other studies: 240 SVs from 48 studies. See in: genome view    
    Remapped(Score: Perfect):31,055,587-31,085,051Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6797723Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr631,087,81031,117,274
    nsv6797723RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr631,055,58731,085,051

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18711336duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18711336Submitted genomicNC_000006.12:g.310
    87810_31117274dup
    GRCh38 (hg38)NC_000006.12Chr631,087,81031,117,274
    nssv18711336RemappedPerfectNC_000006.11:g.310
    55587_31085051dup
    GRCh37.p13First PassNC_000006.11Chr631,055,58731,085,051

    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)
    nssv187113363.9e-0511275330
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