U.S. flag

An official website of the United States government

nsv7041600

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,342

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 122 SVs from 25 studies. See in: genome view    
    Submitted genomic108,530,591-108,545,932Question Mark
    Overlapping variant regions from other studies: 122 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):109,451,747-109,467,088Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7041600Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4108,530,591108,545,932
    nsv7041600RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4109,451,747109,467,088

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18772403inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18772403Submitted genomicNC_000004.12:g.108
    530591_108545932in
    v
    GRCh38 (hg38)NC_000004.12Chr4108,530,591108,545,932
    nssv18772403RemappedPerfectNC_000004.11:g.109
    451747_109467088in
    v
    GRCh37.p13First PassNC_000004.11Chr4109,451,747109,467,088

    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)
    nssv187724034e-061276268
    Support Center