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nsv6909872

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,080

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 90 SVs from 28 studies. See in: genome view    
    Submitted genomic16,870,318-16,883,397Question Mark
    Overlapping variant regions from other studies: 90 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):16,891,865-16,904,944Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6909872Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1116,870,31816,883,397
    nsv6909872RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1116,891,86516,904,944

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18582120duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18582120Submitted genomicNC_000011.10:g.168
    70318_16883397dup
    GRCh38 (hg38)NC_000011.10Chr1116,870,31816,883,397
    nssv18582120RemappedPerfectNC_000011.9:g.1689
    1865_16904944dup
    GRCh37.p13First PassNC_000011.9Chr1116,891,86516,904,944

    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)
    nssv185821204e-061275932
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