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nsv7029830

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:696,167

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2423 SVs from 94 studies. See in: genome view    
    Submitted genomic24,393,949-25,090,115Question Mark
    Overlapping variant regions from other studies: 2423 SVs from 94 studies. See in: genome view    
    Remapped(Score: Perfect):24,789,917-25,486,082Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7029830Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2224,393,94925,090,115
    nsv7029830RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2224,789,91725,486,082

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18651789duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18651789Submitted genomicNC_000022.11:g.243
    93949_25090115dup
    GRCh38 (hg38)NC_000022.11Chr2224,393,94925,090,115
    nssv18651789RemappedPerfectNC_000022.10:g.247
    89917_25486082dup
    GRCh37.p13First PassNC_000022.10Chr2224,789,91725,486,082

    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)
    nssv186517894e-061276010
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