U.S. flag

An official website of the United States government

nsv6646744

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:379,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1468 SVs from 95 studies. See in: genome view    
    Submitted genomic21,707,701-22,087,100Question Mark
    Overlapping variant regions from other studies: 1468 SVs from 95 studies. See in: genome view    
    Remapped(Score: Perfect):22,034,194-22,413,593Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6646744Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr121,707,70122,087,100
    nsv6646744RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr122,034,19422,413,593

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18608688duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18608688Submitted genomicNC_000001.11:g.217
    07701_22087100dup
    GRCh38 (hg38)NC_000001.11Chr121,707,70122,087,100
    nssv18608688RemappedPerfectNC_000001.10:g.220
    34194_22413593dup
    GRCh37.p13First PassNC_000001.10Chr122,034,19422,413,593

    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)
    nssv186086887e-062274460
    Support Center