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nsv6364360

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 20 studies. See in: genome view    
    Submitted genomic141,805,801-141,807,500Question Mark
    Overlapping variant regions from other studies: 104 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):141,524,643-141,526,342Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6364360Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3141,805,801141,807,500
    nsv6364360RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3141,524,643141,526,342

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18094319deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18094319Submitted genomicNC_000003.12:g.141
    805801_141807500de
    l
    GRCh38 (hg38)NC_000003.12Chr3141,805,801141,807,500
    nssv18094319RemappedPerfectNC_000003.11:g.141
    524643_141526342de
    l
    GRCh37.p13First PassNC_000003.11Chr3141,524,643141,526,342

    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)
    nssv18094319<0.001138886
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