U.S. flag

An official website of the United States government

nsv6645520

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35,868

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 198 SVs from 37 studies. See in: genome view    
    Submitted genomic182,617,084-182,652,951Question Mark
    Overlapping variant regions from other studies: 200 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):182,586,219-182,622,086Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6645520Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1182,617,084182,652,951
    nsv6645520RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1182,586,219182,622,086

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18586747duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18586747Submitted genomicNC_000001.11:g.182
    617084_182652951du
    p
    GRCh38 (hg38)NC_000001.11Chr1182,617,084182,652,951
    nssv18586747RemappedPerfectNC_000001.10:g.182
    586219_182622086du
    p
    GRCh37.p13First PassNC_000001.10Chr1182,586,219182,622,086

    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)
    nssv185867471.4e-054275854
    Support Center