U.S. flag

An official website of the United States government

nsv6734042

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,243

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 186 SVs from 30 studies. See in: genome view    
    Submitted genomic20,676,573-20,694,815Question Mark
    Overlapping variant regions from other studies: 186 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):20,678,196-20,696,438Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6734042Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr420,676,57320,694,815
    nsv6734042RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr420,678,19620,696,438

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18495759deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18495759Submitted genomicNC_000004.12:g.206
    76573_20694815del
    GRCh38 (hg38)NC_000004.12Chr420,676,57320,694,815
    nssv18495759RemappedPerfectNC_000004.11:g.206
    78196_20696438del
    GRCh37.p13First PassNC_000004.11Chr420,678,19620,696,438

    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)
    nssv18495759<0.00185276094
    Support Center