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nsv6853317

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:93,349

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 293 SVs from 38 studies. See in: genome view    
    Submitted genomic97,372,288-97,465,636Question Mark
    Overlapping variant regions from other studies: 293 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):98,384,516-98,477,864Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6853317Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr897,372,28897,465,636
    nsv6853317RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr898,384,51698,477,864

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18746138duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18746138Submitted genomicNC_000008.11:g.973
    72288_97465636dup
    GRCh38 (hg38)NC_000008.11Chr897,372,28897,465,636
    nssv18746138RemappedPerfectNC_000008.10:g.983
    84516_98477864dup
    GRCh37.p13First PassNC_000008.10Chr898,384,51698,477,864

    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)
    nssv187461383.6e-0510274562
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