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nsv7025899

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:93

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 178 SVs from 27 studies. See in: genome view    
    Submitted genomic39,719,431-39,719,523Question Mark
    Overlapping variant regions from other studies: 179 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):41,091,358-41,091,450Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7025899Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2139,719,43139,719,523
    nsv7025899RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2141,091,35841,091,450

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18643982duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18643982Submitted genomicNC_000021.9:g.3971
    9431_39719523dup
    GRCh38 (hg38)NC_000021.9Chr2139,719,43139,719,523
    nssv18643982RemappedPerfectNC_000021.8:g.4109
    1358_41091450dup
    GRCh37.p13First PassNC_000021.8Chr2141,091,35841,091,450

    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)
    nssv18643982<0.001143221286
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