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nsv7010990

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:259,070

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1135 SVs from 76 studies. See in: genome view    
    Submitted genomic5,460,102-5,719,171Question Mark
    Overlapping variant regions from other studies: 1135 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):5,440,748-5,699,817Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7010990Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr205,460,1025,719,171
    nsv7010990RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr205,440,7485,699,817

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18644397duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18644397Submitted genomicNC_000020.11:g.546
    0102_5719171dup
    GRCh38 (hg38)NC_000020.11Chr205,460,1025,719,171
    nssv18644397RemappedPerfectNC_000020.10:g.544
    0748_5699817dup
    GRCh37.p13First PassNC_000020.10Chr205,440,7485,699,817

    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)
    nssv186443974e-061275786
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