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nsv7086371

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:434,696

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 812 SVs from 61 studies. See in: genome view    
    Submitted genomic25,824,703-26,259,398Question Mark
    Overlapping variant regions from other studies: 813 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):25,842,820-26,277,515Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7086371Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX25,824,70326,259,398
    nsv7086371RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX25,842,82026,277,515

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18655267duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18655267Submitted genomicNC_000023.11:g.258
    24703_26259398dup
    GRCh38 (hg38)NC_000023.11ChrX25,824,70326,259,398
    nssv18655267RemappedPerfectNC_000023.10:g.258
    42820_26277515dup
    GRCh37.p13First PassNC_000023.10ChrX25,842,82026,277,515

    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)
    nssv186552675e-061200000
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