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nsv7085466

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:68,721

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 482 SVs from 43 studies. See in: genome view    
    Submitted genomic15,205,544-15,274,264Question Mark
    Overlapping variant regions from other studies: 483 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):15,223,666-15,292,386Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7085466Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX15,205,54415,274,264
    nsv7085466RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX15,223,66615,292,386

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18654522duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18654522Submitted genomicNC_000023.11:g.152
    05544_15274264dup
    GRCh38 (hg38)NC_000023.11ChrX15,205,54415,274,264
    nssv18654522RemappedPerfectNC_000023.10:g.152
    23666_15292386dup
    GRCh37.p13First PassNC_000023.10ChrX15,223,66615,292,386

    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)
    nssv186545225e-061200000
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