U.S. flag

An official website of the United States government

nsv6316727

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,804

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 85 SVs from 19 studies. See in: genome view    
    Submitted genomic32,324,573-32,326,376Question Mark
    Overlapping variant regions from other studies: 85 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):32,790,174-32,791,977Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6316727Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr132,324,57332,326,376
    nsv6316727RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr132,790,17432,791,977

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18060447deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18060447Submitted genomicNC_000001.11:g.323
    24573_32326376del
    GRCh38 (hg38)NC_000001.11Chr132,324,57332,326,376
    nssv18060447RemappedPerfectNC_000001.10:g.327
    90174_32791977del
    GRCh37.p13First PassNC_000001.10Chr132,790,17432,791,977

    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)
    nssv18060447<0.001138824
    Support Center