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nsv6668439

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:411,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1133 SVs from 90 studies. See in: genome view    
    Submitted genomic228,005,301-228,416,300Question Mark
    Overlapping variant regions from other studies: 1136 SVs from 90 studies. See in: genome view    
    Remapped(Score: Perfect):228,193,002-228,604,001Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6668439Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1228,005,301228,416,300
    nsv6668439RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1228,193,002228,604,001

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18609399duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18609399Submitted genomicNC_000001.11:g.228
    005301_228416300du
    p
    GRCh38 (hg38)NC_000001.11Chr1228,005,301228,416,300
    nssv18609399RemappedPerfectNC_000001.10:g.228
    193002_228604001du
    p
    GRCh37.p13First PassNC_000001.10Chr1228,193,002228,604,001

    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)
    nssv186093994e-061265402
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