U.S. flag

An official website of the United States government

nsv7052079

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,471,001

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7998 SVs from 108 studies. See in: genome view    
    Submitted genomic119,644,000-123,115,000Question Mark
    Overlapping variant regions from other studies: 7998 SVs from 108 studies. See in: genome view    
    Remapped(Score: Perfect):119,965,161-123,436,145Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052079Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6119,644,000123,115,000
    nsv7052079RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6119,965,161123,436,145

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18778351inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18778351Submitted genomicNC_000006.12:g.119
    644000_123115000in
    v
    GRCh38 (hg38)NC_000006.12Chr6119,644,000123,115,000
    nssv18778351RemappedPerfectNC_000006.11:g.119
    965161_123436145in
    v
    GRCh37.p13First PassNC_000006.11Chr6119,965,161123,436,145

    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)
    nssv187783514e-061276268
    Support Center