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nsv6898516

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:50,264

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 283 SVs from 35 studies. See in: genome view    
    Submitted genomic129,835,330-129,885,593Question Mark
    Overlapping variant regions from other studies: 283 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):129,705,225-129,755,488Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6898516Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11129,835,330129,885,593
    nsv6898516RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11129,705,225129,755,488

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18583510duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18583510Submitted genomicNC_000011.10:g.129
    835330_129885593du
    p
    GRCh38 (hg38)NC_000011.10Chr11129,835,330129,885,593
    nssv18583510RemappedPerfectNC_000011.9:g.1297
    05225_129755488dup
    GRCh37.p13First PassNC_000011.9Chr11129,705,225129,755,488

    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)
    nssv185835101.4e-054275788
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