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nsv6980129

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:127,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 541 SVs from 74 studies. See in: genome view    
    Submitted genomic86,464,201-86,591,400Question Mark
    Overlapping variant regions from other studies: 541 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):86,497,807-86,625,006Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6980129Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1686,464,20186,591,400
    nsv6980129RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1686,497,80786,625,006

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18625416duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18625416Submitted genomicNC_000016.10:g.864
    64201_86591400dup
    GRCh38 (hg38)NC_000016.10Chr1686,464,20186,591,400
    nssv18625416RemappedPerfectNC_000016.9:g.8649
    7807_86625006dup
    GRCh37.p13First PassNC_000016.9Chr1686,497,80786,625,006

    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)
    nssv186254164e-061274576
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