U.S. flag

An official website of the United States government

nsv6702886

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:228

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 108 SVs from 27 studies. See in: genome view    
    Submitted genomic11,754,827-11,755,054Question Mark
    Overlapping variant regions from other studies: 108 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):11,796,301-11,796,528Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6702886Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr311,754,82711,755,054
    nsv6702886RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr311,796,30111,796,528

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18669718duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18669718Submitted genomicNC_000003.12:g.117
    54827_11755054dup
    GRCh38 (hg38)NC_000003.12Chr311,754,82711,755,054
    nssv18669718RemappedPerfectNC_000003.11:g.117
    96301_11796528dup
    GRCh37.p13First PassNC_000003.11Chr311,796,30111,796,528

    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)
    nssv186697189.7e-0523231676
    Support Center