U.S. flag

An official website of the United States government

nsv6590746

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:221,832

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 806 SVs from 69 studies. See in: genome view    
    Submitted genomic132,900,493-133,122,324Question Mark
    Overlapping variant regions from other studies: 806 SVs from 69 studies. See in: genome view    
    Remapped(Score: Perfect):133,477,079-133,698,910Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6590746Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12132,900,493133,122,324
    nsv6590746RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12133,477,079133,698,910

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18234022inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18234022Submitted genomicNC_000012.12:g.132
    900493_133122324in
    v
    GRCh38 (hg38)NC_000012.12Chr12132,900,493133,122,324
    nssv18234022RemappedPerfectNC_000012.11:g.133
    477079_133698910in
    v
    GRCh37.p13First PassNC_000012.11Chr12133,477,079133,698,910

    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)
    nssv18234022<0.001139304
    Support Center