U.S. flag

An official website of the United States government

nsv6783952

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:182,234

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2843 SVs from 105 studies. See in: genome view    
    Submitted genomic31,140,741-31,322,974Question Mark
    Overlapping variant regions from other studies: 2843 SVs from 105 studies. See in: genome view    
    Remapped(Score: Perfect):31,108,518-31,290,751Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6783952Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr631,140,74131,322,974
    nsv6783952RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr631,108,51831,290,751

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18711338duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18711338Submitted genomicNC_000006.12:g.311
    40741_31322974dup
    GRCh38 (hg38)NC_000006.12Chr631,140,74131,322,974
    nssv18711338RemappedPerfectNC_000006.11:g.311
    08518_31290751dup
    GRCh37.p13First PassNC_000006.11Chr631,108,51831,290,751

    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)
    nssv187113384e-061268726
    Support Center