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nsv6793206

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19,311

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 120 SVs from 20 studies. See in: genome view    
    Submitted genomic147,579,417-147,598,727Question Mark
    Overlapping variant regions from other studies: 120 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):146,958,980-146,978,290Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6793206Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5147,579,417147,598,727
    nsv6793206RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5146,958,980146,978,290

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18700445duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18700445Submitted genomicNC_000005.10:g.147
    579417_147598727du
    p
    GRCh38 (hg38)NC_000005.10Chr5147,579,417147,598,727
    nssv18700445RemappedPerfectNC_000005.9:g.1469
    58980_146978290dup
    GRCh37.p13First PassNC_000005.9Chr5146,958,980146,978,290

    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)
    nssv187004454e-061275714
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