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nsv6682376

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:29,658

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 160 SVs from 35 studies. See in: genome view    
    Submitted genomic228,495,216-228,524,873Question Mark
    Overlapping variant regions from other studies: 160 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):229,359,932-229,389,589Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6682376Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2228,495,216228,524,873
    nsv6682376RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2229,359,932229,389,589

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18662052duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18662052Submitted genomicNC_000002.12:g.228
    495216_228524873du
    p
    GRCh38 (hg38)NC_000002.12Chr2228,495,216228,524,873
    nssv18662052RemappedPerfectNC_000002.11:g.229
    359932_229389589du
    p
    GRCh37.p13First PassNC_000002.11Chr2229,359,932229,389,589

    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)
    nssv186620524e-061274500
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