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nsv6926616

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:31,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 204 SVs from 43 studies. See in: genome view    
    Submitted genomic9,928,201-9,959,500Question Mark
    Overlapping variant regions from other studies: 205 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):10,080,800-10,112,099Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6926616Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr129,928,2019,959,500
    nsv6926616RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1210,080,80010,112,099

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18599110duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18599110Submitted genomicNC_000012.12:g.992
    8201_9959500dup
    GRCh38 (hg38)NC_000012.12Chr129,928,2019,959,500
    nssv18599110RemappedPerfectNC_000012.11:g.100
    80800_10112099dup
    GRCh37.p13First PassNC_000012.11Chr1210,080,80010,112,099

    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)
    nssv185991107.1e-0520274434
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