U.S. flag

An official website of the United States government

nsv6789669

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:764,087

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2353 SVs from 109 studies. See in: genome view    
    Submitted genomic25,978,117-26,742,203Question Mark
    Overlapping variant regions from other studies: 1682 SVs from 96 studies. See in: genome view    
    Remapped(Score: Pass):25,978,345-26,585,842Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6789669Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr625,978,11726,742,203
    nsv6789669RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr625,978,34526,585,842

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18714036duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18714036Submitted genomicNC_000006.12:g.259
    78117_26742203dup
    GRCh38 (hg38)NC_000006.12Chr625,978,11726,742,203
    nssv18714036RemappedPassNC_000006.11:g.259
    78345_26585842dup
    GRCh37.p13First PassNC_000006.11Chr625,978,34526,585,842

    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)
    nssv187140364e-061259342
    Support Center