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nsv7080562

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:661,656

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 984 SVs from 58 studies. See in: genome view    
    Submitted genomic26,146,788-26,808,443Question Mark
    Overlapping variant regions from other studies: 985 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):26,164,905-26,826,560Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7080562Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX26,146,78826,808,443
    nsv7080562RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX26,164,90526,826,560

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18655297duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18655297Submitted genomicNC_000023.11:g.261
    46788_26808443dup
    GRCh38 (hg38)NC_000023.11ChrX26,146,78826,808,443
    nssv18655297RemappedPerfectNC_000023.10:g.261
    64905_26826560dup
    GRCh37.p13First PassNC_000023.10ChrX26,164,90526,826,560

    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)
    nssv186552975e-061200000
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