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nsv6422995

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:493

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 141 SVs from 15 studies. See in: genome view    
    Submitted genomic38,035,321-38,035,813Question Mark
    Overlapping variant regions from other studies: 141 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):37,892,839-37,893,331Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6422995Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr838,035,32138,035,813
    nsv6422995RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr837,892,83937,893,331

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18168922deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18168922Submitted genomicNC_000008.11:g.380
    35321_38035813del
    GRCh38 (hg38)NC_000008.11Chr838,035,32138,035,813
    nssv18168922RemappedPerfectNC_000008.10:g.378
    92839_37893331del
    GRCh37.p13First PassNC_000008.10Chr837,892,83937,893,331

    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)
    nssv18168922<0.001434952
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