U.S. flag

An official website of the United States government

nsv7021157

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,264,184

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7313 SVs from 84 studies. See in: genome view    
    Submitted genomic14,244,684-19,508,867Question Mark
    Overlapping variant regions from other studies: 7315 SVs from 84 studies. See in: genome view    
    Remapped(Score: Perfect):14,262,806-19,526,985Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7021157Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX14,244,68419,508,867
    nsv7021157RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX14,262,80619,526,985

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18763388inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18763388Submitted genomicNC_000023.11:g.142
    44684_19508867inv
    GRCh38 (hg38)NC_000023.11ChrX14,244,68419,508,867
    nssv18763388RemappedPerfectNC_000023.10:g.142
    62806_19526985inv
    GRCh37.p13First PassNC_000023.10ChrX14,262,80619,526,985

    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)
    nssv187633885e-061200000
    Support Center