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nsv6989721

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:78

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 96 SVs from 30 studies. See in: genome view    
    Submitted genomic18,851,906-18,851,983Question Mark
    Overlapping variant regions from other studies: 96 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):18,863,228-18,863,305Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6989721Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1618,851,90618,851,983
    nsv6989721RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1618,863,22818,863,305

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18619971duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18619971Submitted genomicNC_000016.10:g.188
    51906_18851983dup
    GRCh38 (hg38)NC_000016.10Chr1618,851,90618,851,983
    nssv18619971RemappedPerfectNC_000016.9:g.1886
    3228_18863305dup
    GRCh37.p13First PassNC_000016.9Chr1618,863,22818,863,305

    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)
    nssv18619971<0.00158223022
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