U.S. flag

An official website of the United States government

nsv6968087

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 168 SVs from 35 studies. See in: genome view    
    Submitted genomic103,909,601-103,919,000Question Mark
    Overlapping variant regions from other studies: 168 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):104,375,938-104,385,337Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6968087Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr14103,909,601103,919,000
    nsv6968087RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr14104,375,938104,385,337

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18383621deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18383621Submitted genomicNC_000014.9:g.1039
    09601_103919000del
    GRCh38 (hg38)NC_000014.9Chr14103,909,601103,919,000
    nssv18383621RemappedPerfectNC_000014.8:g.1043
    75938_104385337del
    GRCh37.p13First PassNC_000014.8Chr14104,375,938104,385,337

    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)
    nssv183836214e-061276166
    Support Center