U.S. flag

An official website of the United States government

nsv6747441

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,587

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 25 studies. See in: genome view    
    Submitted genomic109,932,359-109,935,945Question Mark
    Overlapping variant regions from other studies: 104 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):110,853,515-110,857,101Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6747441Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4109,932,359109,935,945
    nsv6747441RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4110,853,515110,857,101

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18485652deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18485652Submitted genomicNC_000004.12:g.109
    932359_109935945de
    l
    GRCh38 (hg38)NC_000004.12Chr4109,932,359109,935,945
    nssv18485652RemappedPerfectNC_000004.11:g.110
    853515_110857101de
    l
    GRCh37.p13First PassNC_000004.11Chr4110,853,515110,857,101

    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)
    nssv184856524e-061276012
    Support Center