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nsv7082038

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,311

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 279 SVs from 25 studies. See in: genome view    
    Submitted genomic97,502,023-97,509,333Question Mark
    Overlapping variant regions from other studies: 279 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):96,757,022-96,764,332Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7082038Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX97,502,02397,509,333
    nsv7082038RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX96,757,02296,764,332

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18658712duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18658712Submitted genomicNC_000023.11:g.975
    02023_97509333dup
    GRCh38 (hg38)NC_000023.11ChrX97,502,02397,509,333
    nssv18658712RemappedPerfectNC_000023.10:g.967
    57022_96764332dup
    GRCh37.p13First PassNC_000023.10ChrX96,757,02296,764,332

    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)
    nssv186587121.4e-053214286
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