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nsv6734376

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20,674

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 357 SVs from 57 studies. See in: genome view    
    Submitted genomic197,491,684-197,512,357Question Mark
    Overlapping variant regions from other studies: 357 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):197,218,555-197,239,228Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6734376Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3197,491,684197,512,357
    nsv6734376RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3197,218,555197,239,228

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18480135deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18480135Submitted genomicNC_000003.12:g.197
    491684_197512357de
    l
    GRCh38 (hg38)NC_000003.12Chr3197,491,684197,512,357
    nssv18480135RemappedPerfectNC_000003.11:g.197
    218555_197239228de
    l
    GRCh37.p13First PassNC_000003.11Chr3197,218,555197,239,228

    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)
    nssv184801354.3e-0512275864
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