U.S. flag

An official website of the United States government

nsv6751365

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:120,928

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 356 SVs from 43 studies. See in: genome view    
    Submitted genomic67,669,276-67,790,203Question Mark
    Overlapping variant regions from other studies: 356 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):68,534,994-68,655,921Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6751365Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr467,669,27667,790,203
    nsv6751365RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr468,534,99468,655,921

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18692007duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18692007Submitted genomicNC_000004.12:g.676
    69276_67790203dup
    GRCh38 (hg38)NC_000004.12Chr467,669,27667,790,203
    nssv18692007RemappedPerfectNC_000004.11:g.685
    34994_68655921dup
    GRCh37.p13First PassNC_000004.11Chr468,534,99468,655,921

    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)
    nssv186920071.1e-053274456
    Support Center