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nsv6843109

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:22,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 129 SVs from 25 studies. See in: genome view    
    Submitted genomic64,581,901-64,604,300Question Mark
    Overlapping variant regions from other studies: 129 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):65,494,458-65,516,857Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6843109Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr864,581,90164,604,300
    nsv6843109RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr865,494,45865,516,857

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18731031duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18731031Submitted genomicNC_000008.11:g.645
    81901_64604300dup
    GRCh38 (hg38)NC_000008.11Chr864,581,90164,604,300
    nssv18731031RemappedPerfectNC_000008.10:g.654
    94458_65516857dup
    GRCh37.p13First PassNC_000008.10Chr865,494,45865,516,857

    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)
    nssv187310315.4e-0515273562
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