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nsv6838589

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:80,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 534 SVs from 53 studies. See in: genome view    
    Submitted genomic94,697,701-94,778,200Question Mark
    Overlapping variant regions from other studies: 534 SVs from 53 studies. See in: genome view    
    Remapped(Score: Perfect):95,709,929-95,790,428Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6838589Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr894,697,70194,778,200
    nsv6838589RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr895,709,92995,790,428

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18749917duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18749917Submitted genomicNC_000008.11:g.946
    97701_94778200dup
    GRCh38 (hg38)NC_000008.11Chr894,697,70194,778,200
    nssv18749917RemappedPerfectNC_000008.10:g.957
    09929_95790428dup
    GRCh37.p13First PassNC_000008.10Chr895,709,92995,790,428

    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)
    nssv187499175.4e-0515273958
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