U.S. flag

An official website of the United States government

nsv7089904

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,468

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 246 SVs from 19 studies. See in: genome view    
    Submitted genomic84,128,632-84,131,099Question Mark
    Overlapping variant regions from other studies: 246 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):83,383,640-83,386,107Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7089904Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX84,128,63284,131,099
    nsv7089904RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX83,383,64083,386,107

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18456275deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18456275Submitted genomicNC_000023.11:g.841
    28632_84131099del
    GRCh38 (hg38)NC_000023.11ChrX84,128,63284,131,099
    nssv18456275RemappedPerfectNC_000023.10:g.833
    83640_83386107del
    GRCh37.p13First PassNC_000023.10ChrX83,383,64083,386,107

    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)
    nssv184562755e-061200000
    Support Center