U.S. flag

An official website of the United States government

nsv7055574

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,222

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 243 SVs from 31 studies. See in: genome view    
    Submitted genomic184,121,410-184,122,631Question Mark
    Overlapping variant regions from other studies: 243 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):185,042,563-185,043,784Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7055574Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4184,121,410184,122,631
    nsv7055574RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4185,042,563185,043,784

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18773990inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18773990Submitted genomicNC_000004.12:g.184
    121410_184122631in
    v
    GRCh38 (hg38)NC_000004.12Chr4184,121,410184,122,631
    nssv18773990RemappedPerfectNC_000004.11:g.185
    042563_185043784in
    v
    GRCh37.p13First PassNC_000004.11Chr4185,042,563185,043,784

    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)
    nssv187739904e-061276268
    Support Center