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nsv6850367

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:43,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 325 SVs from 55 studies. See in: genome view    
    Submitted genomic22,353,101-22,396,600Question Mark
    Overlapping variant regions from other studies: 325 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):22,210,614-22,254,113Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6850367Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr822,353,10122,396,600
    nsv6850367RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr822,210,61422,254,113

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18747712duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18747712Submitted genomicNC_000008.11:g.223
    53101_22396600dup
    GRCh38 (hg38)NC_000008.11Chr822,353,10122,396,600
    nssv18747712RemappedPerfectNC_000008.10:g.222
    10614_22254113dup
    GRCh37.p13First PassNC_000008.10Chr822,210,61422,254,113

    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)
    nssv187477124e-061275480
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