U.S. flag

An official website of the United States government

nsv6664968

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:628,289

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1450 SVs from 79 studies. See in: genome view    
    Submitted genomic63,553,509-64,181,797Question Mark
    Overlapping variant regions from other studies: 1450 SVs from 79 studies. See in: genome view    
    Remapped(Score: Perfect):63,780,643-64,408,931Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6664968Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr263,553,50964,181,797
    nsv6664968RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr263,780,64364,408,931

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18666076duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18666076Submitted genomicNC_000002.12:g.635
    53509_64181797dup
    GRCh38 (hg38)NC_000002.12Chr263,553,50964,181,797
    nssv18666076RemappedPerfectNC_000002.11:g.637
    80643_64408931dup
    GRCh37.p13First PassNC_000002.11Chr263,780,64364,408,931

    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)
    nssv186660764e-061274680
    Support Center