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nsv6870021

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:71,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 520 SVs from 61 studies. See in: genome view    
    Submitted genomic140,442,301-140,514,200Question Mark
    Overlapping variant regions from other studies: 520 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):141,452,400-141,524,299Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6870021Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8140,442,301140,514,200
    nsv6870021RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8141,452,400141,524,299

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18742675duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18742675Submitted genomicNC_000008.11:g.140
    442301_140514200du
    p
    GRCh38 (hg38)NC_000008.11Chr8140,442,301140,514,200
    nssv18742675RemappedPerfectNC_000008.10:g.141
    452400_141524299du
    p
    GRCh37.p13First PassNC_000008.10Chr8141,452,400141,524,299

    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)
    nssv18742675<0.00138263938
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