U.S. flag

An official website of the United States government

nsv6718526

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,183

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 188 SVs from 39 studies. See in: genome view    
    Submitted genomic194,310,593-194,328,775Question Mark
    Overlapping variant regions from other studies: 164 SVs from 42 studies. See in: genome view    
    Remapped(Score: Pass):194,028,382-194,049,504Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6718526Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3194,310,593194,328,775
    nsv6718526RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3194,028,382194,049,504

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18478228deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18478228Submitted genomicNC_000003.12:g.194
    310593_194328775de
    l
    GRCh38 (hg38)NC_000003.12Chr3194,310,593194,328,775
    nssv18478228RemappedPassNC_000003.11:g.194
    028382_194049504de
    l
    GRCh37.p13First PassNC_000003.11Chr3194,028,382194,049,504

    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)
    nssv184782281.1e-053276104
    Support Center