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nsv7085225

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,863

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 283 SVs from 20 studies. See in: genome view    
    Submitted genomic14,820,378-14,825,240Question Mark
    Overlapping variant regions from other studies: 284 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):14,838,500-14,843,362Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7085225Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX14,820,37814,825,240
    nsv7085225RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX14,838,50014,843,362

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18459249deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18459249Submitted genomicNC_000023.11:g.148
    20378_14825240del
    GRCh38 (hg38)NC_000023.11ChrX14,820,37814,825,240
    nssv18459249RemappedPerfectNC_000023.10:g.148
    38500_14843362del
    GRCh37.p13First PassNC_000023.10ChrX14,838,50014,843,362

    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)
    nssv184592495e-061200000
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