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nsv6800254

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:146,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 517 SVs from 55 studies. See in: genome view    
    Submitted genomic165,868,701-166,015,600Question Mark
    Overlapping variant regions from other studies: 517 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):166,282,189-166,429,088Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6800254Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6165,868,701166,015,600
    nsv6800254RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6166,282,189166,429,088

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18714604duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18714604Submitted genomicNC_000006.12:g.165
    868701_166015600du
    p
    GRCh38 (hg38)NC_000006.12Chr6165,868,701166,015,600
    nssv18714604RemappedPerfectNC_000006.11:g.166
    282189_166429088du
    p
    GRCh37.p13First PassNC_000006.11Chr6166,282,189166,429,088

    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)
    nssv187146042.5e-057269900
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