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nsv6676218

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:260

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 90 SVs from 15 studies. See in: genome view    
    Submitted genomic14,345,730-14,345,989Question Mark
    Overlapping variant regions from other studies: 90 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):14,485,854-14,486,113Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6676218Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr214,345,73014,345,989
    nsv6676218RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr214,485,85414,486,113

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18650620duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18650620Submitted genomicNC_000002.12:g.143
    45730_14345989dup
    GRCh38 (hg38)NC_000002.12Chr214,345,73014,345,989
    nssv18650620RemappedPerfectNC_000002.11:g.144
    85854_14486113dup
    GRCh37.p13First PassNC_000002.11Chr214,485,85414,486,113

    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)
    nssv186506204e-061239284
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