U.S. flag

An official website of the United States government

nsv6332383

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,010

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 155 SVs from 25 studies. See in: genome view    
    Submitted genomic42,980,592-42,987,601Question Mark
    Overlapping variant regions from other studies: 155 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):43,446,263-43,453,272Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6332383Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr142,980,59242,987,601
    nsv6332383RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr143,446,26343,453,272

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18060513deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18060513Submitted genomicNC_000001.11:g.429
    80592_42987601del
    GRCh38 (hg38)NC_000001.11Chr142,980,59242,987,601
    nssv18060513RemappedPerfectNC_000001.10:g.434
    46263_43453272del
    GRCh37.p13First PassNC_000001.10Chr143,446,26343,453,272

    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)
    nssv18060513<0.0011439304
    Support Center