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nsv6746690

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:341,056

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1671 SVs from 94 studies. See in: genome view    
    Submitted genomic143,819,431-144,160,486Question Mark
    Overlapping variant regions from other studies: 1671 SVs from 94 studies. See in: genome view    
    Remapped(Score: Perfect):144,740,584-145,081,639Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6746690Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4143,819,431144,160,486
    nsv6746690RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4144,740,584145,081,639

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18683959duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18683959Submitted genomicNC_000004.12:g.143
    819431_144160486du
    p
    GRCh38 (hg38)NC_000004.12Chr4143,819,431144,160,486
    nssv18683959RemappedPerfectNC_000004.11:g.144
    740584_145081639du
    p
    GRCh37.p13First PassNC_000004.11Chr4144,740,584145,081,639

    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)
    nssv186839597e-062269772
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