U.S. flag

An official website of the United States government

nsv6867018

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:139,945

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 656 SVs from 73 studies. See in: genome view    
    Submitted genomic94,517,455-94,657,399Question Mark
    Overlapping variant regions from other studies: 656 SVs from 73 studies. See in: genome view    
    Remapped(Score: Perfect):97,279,737-97,419,681Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6867018Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr994,517,45594,657,399
    nsv6867018RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr997,279,73797,419,681

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18738496duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18738496Submitted genomicNC_000009.12:g.945
    17455_94657399dup
    GRCh38 (hg38)NC_000009.12Chr994,517,45594,657,399
    nssv18738496RemappedPerfectNC_000009.11:g.972
    79737_97419681dup
    GRCh37.p13First PassNC_000009.11Chr997,279,73797,419,681

    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)
    nssv187384964e-061274344
    Support Center