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nsv7029866

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:56

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 258 SVs from 36 studies. See in: genome view    
    Submitted genomic23,750,966-23,751,021Question Mark
    Overlapping variant regions from other studies: 258 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):24,093,153-24,093,208Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7029866Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2223,750,96623,751,021
    nsv7029866RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2224,093,15324,093,208

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18651423duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18651423Submitted genomicNC_000022.11:g.237
    50966_23751021dup
    GRCh38 (hg38)NC_000022.11Chr2223,750,96623,751,021
    nssv18651423RemappedPerfectNC_000022.10:g.240
    93153_24093208dup
    GRCh37.p13First PassNC_000022.10Chr2224,093,15324,093,208

    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)
    nssv186514230.003514185404
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