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nsv6963455

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,481

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 103 SVs from 20 studies. See in: genome view    
    Submitted genomic102,051,900-102,056,380Question Mark
    Overlapping variant regions from other studies: 103 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):102,518,237-102,522,717Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6963455Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr14102,051,900102,056,380
    nsv6963455RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr14102,518,237102,522,717

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18383421deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18383421Submitted genomicNC_000014.9:g.1020
    51900_102056380del
    GRCh38 (hg38)NC_000014.9Chr14102,051,900102,056,380
    nssv18383421RemappedPerfectNC_000014.8:g.1025
    18237_102522717del
    GRCh37.p13First PassNC_000014.8Chr14102,518,237102,522,717

    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)
    nssv183834214e-061273480
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