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nsv6333941

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:659

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 106 SVs from 17 studies. See in: genome view    
    Submitted genomic93,463,661-93,464,319Question Mark
    Overlapping variant regions from other studies: 106 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):93,929,218-93,929,876Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6333941Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr193,463,66193,464,319
    nsv6333941RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr193,929,21893,929,876

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18065569deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18065569Submitted genomicNC_000001.11:g.934
    63661_93464319del
    GRCh38 (hg38)NC_000001.11Chr193,463,66193,464,319
    nssv18065569RemappedPerfectNC_000001.10:g.939
    29218_93929876del
    GRCh37.p13First PassNC_000001.10Chr193,929,21893,929,876

    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)
    nssv18065569<0.001538358
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