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nsv7080559

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:530,929

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 812 SVs from 56 studies. See in: genome view    
    Submitted genomic26,129,076-26,660,004Question Mark
    Overlapping variant regions from other studies: 813 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):26,147,193-26,678,121Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7080559Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX26,129,07626,660,004
    nsv7080559RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX26,147,19326,678,121

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18655294duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18655294Submitted genomicNC_000023.11:g.261
    29076_26660004dup
    GRCh38 (hg38)NC_000023.11ChrX26,129,07626,660,004
    nssv18655294RemappedPerfectNC_000023.10:g.261
    47193_26678121dup
    GRCh37.p13First PassNC_000023.10ChrX26,147,19326,678,121

    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)
    nssv186552945e-061200000
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