U.S. flag

An official website of the United States government

nsv6722104

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:38,255

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 427 SVs from 54 studies. See in: genome view    
    Submitted genomic2,747,477-2,785,731Question Mark
    Overlapping variant regions from other studies: 427 SVs from 54 studies. See in: genome view    
    Remapped(Score: Perfect):2,749,204-2,787,458Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6722104Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr42,747,4772,785,731
    nsv6722104RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr42,749,2042,787,458

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18689418duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18689418Submitted genomicNC_000004.12:g.274
    7477_2785731dup
    GRCh38 (hg38)NC_000004.12Chr42,747,4772,785,731
    nssv18689418RemappedPerfectNC_000004.11:g.274
    9204_2787458dup
    GRCh37.p13First PassNC_000004.11Chr42,749,2042,787,458

    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)
    nssv186894184e-061275828
    Support Center