U.S. flag

An official website of the United States government

nsv7053613

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,013

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 247 SVs from 22 studies. See in: genome view    
    Submitted genomic88,983,657-88,984,669Question Mark
    Overlapping variant regions from other studies: 247 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):88,238,658-88,239,670Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7053613Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX88,983,65788,984,669
    nsv7053613RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX88,238,65888,239,670

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18764522inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18764522Submitted genomicNC_000023.11:g.889
    83657_88984669inv
    GRCh38 (hg38)NC_000023.11ChrX88,983,65788,984,669
    nssv18764522RemappedPerfectNC_000023.10:g.882
    38658_88239670inv
    GRCh37.p13First PassNC_000023.10ChrX88,238,65888,239,670

    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)
    nssv187645221.4e-053214286
    Support Center