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nsv6983353

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:30,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 244 SVs from 40 studies. See in: genome view    
    Submitted genomic59,120,801-59,150,800Question Mark
    Overlapping variant regions from other studies: 243 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):57,198,162-57,228,161Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6983353Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1759,120,80159,150,800
    nsv6983353RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1757,198,16257,228,161

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18627319duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18627319Submitted genomicNC_000017.11:g.591
    20801_59150800dup
    GRCh38 (hg38)NC_000017.11Chr1759,120,80159,150,800
    nssv18627319RemappedPerfectNC_000017.10:g.571
    98162_57228161dup
    GRCh37.p13First PassNC_000017.10Chr1757,198,16257,228,161

    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)
    nssv186273191.9e-055263504
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