U.S. flag

An official website of the United States government

nsv7048818

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,475

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 100 SVs from 26 studies. See in: genome view    
    Submitted genomic227,979,973-227,986,447Question Mark
    Overlapping variant regions from other studies: 100 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):228,844,689-228,851,163Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048818Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2227,979,973227,986,447
    nsv7048818RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2228,844,689228,851,163

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767672inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767672Submitted genomicNC_000002.12:g.227
    979973_227986447in
    v
    GRCh38 (hg38)NC_000002.12Chr2227,979,973227,986,447
    nssv18767672RemappedPerfectNC_000002.11:g.228
    844689_228851163in
    v
    GRCh37.p13First PassNC_000002.11Chr2228,844,689228,851,163

    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)
    nssv187676724e-061276268
    Support Center