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nsv7086237

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 296 SVs from 31 studies. See in: genome view    
    Submitted genomic24,150,001-24,167,200Question Mark
    Overlapping variant regions from other studies: 297 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):24,168,118-24,185,317Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7086237Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX24,150,00124,167,200
    nsv7086237RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX24,168,11824,185,317

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18655208duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18655208Submitted genomicNC_000023.11:g.241
    50001_24167200dup
    GRCh38 (hg38)NC_000023.11ChrX24,150,00124,167,200
    nssv18655208RemappedPerfectNC_000023.10:g.241
    68118_24185317dup
    GRCh37.p13First PassNC_000023.10ChrX24,168,11824,185,317

    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)
    nssv186552085e-061200000
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