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nsv6364255

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,409

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 102 SVs from 20 studies. See in: genome view    
    Submitted genomic141,810,754-141,814,162Question Mark
    Overlapping variant regions from other studies: 102 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):141,529,596-141,533,004Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6364255Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3141,810,754141,814,162
    nsv6364255RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3141,529,596141,533,004

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18094320deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18094320Submitted genomicNC_000003.12:g.141
    810754_141814162de
    l
    GRCh38 (hg38)NC_000003.12Chr3141,810,754141,814,162
    nssv18094320RemappedPerfectNC_000003.11:g.141
    529596_141533004de
    l
    GRCh37.p13First PassNC_000003.11Chr3141,529,596141,533,004

    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)
    nssv18094320<0.001139258
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