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nsv6377667

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 85 SVs from 20 studies. See in: genome view    
    Submitted genomic52,008,501-52,010,100Question Mark
    Overlapping variant regions from other studies: 85 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):52,874,667-52,876,266Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6377667Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr452,008,50152,010,100
    nsv6377667RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr452,874,66752,876,266

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18117312deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18117312Submitted genomicNC_000004.12:g.520
    08501_52010100del
    GRCh38 (hg38)NC_000004.12Chr452,008,50152,010,100
    nssv18117312RemappedPerfectNC_000004.11:g.528
    74667_52876266del
    GRCh37.p13First PassNC_000004.11Chr452,874,66752,876,266

    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)
    nssv18117312<0.001739028
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