U.S. flag

An official website of the United States government

nsv6696501

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:24,145

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 182 SVs from 41 studies. See in: genome view    
    Submitted genomic228,468,937-228,493,081Question Mark
    Overlapping variant regions from other studies: 182 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):229,333,653-229,357,797Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6696501Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2228,468,937228,493,081
    nsv6696501RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2229,333,653229,357,797

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18450224deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18450224Submitted genomicNC_000002.12:g.228
    468937_228493081de
    l
    GRCh38 (hg38)NC_000002.12Chr2228,468,937228,493,081
    nssv18450224RemappedPerfectNC_000002.11:g.229
    333653_229357797de
    l
    GRCh37.p13First PassNC_000002.11Chr2229,333,653229,357,797

    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)
    nssv184502241.4e-054275760
    Support Center