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nsv6321351

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,892

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 86 SVs from 19 studies. See in: genome view    
    Submitted genomic32,288,011-32,293,902Question Mark
    Overlapping variant regions from other studies: 86 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):32,753,612-32,759,503Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6321351Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr132,288,01132,293,902
    nsv6321351RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr132,753,61232,759,503

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18060445deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18060445Submitted genomicNC_000001.11:g.322
    88011_32293902del
    GRCh38 (hg38)NC_000001.11Chr132,288,01132,293,902
    nssv18060445RemappedPerfectNC_000001.10:g.327
    53612_32759503del
    GRCh37.p13First PassNC_000001.10Chr132,753,61232,759,503

    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)
    nssv18060445<0.001139174
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