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nsv7019232

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,259

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 95 SVs from 27 studies. See in: genome view    
    Submitted genomic26,562,529-26,569,787Question Mark
    Overlapping variant regions from other studies: 95 SVs from 27 studies. See in: genome view    
    Remapped(Score: Good):26,958,495-26,965,752Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7019232Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2226,562,52926,569,787
    nsv7019232RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2226,958,49526,965,752

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18436691deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18436691Submitted genomicNC_000022.11:g.265
    62529_26569787del
    GRCh38 (hg38)NC_000022.11Chr2226,562,52926,569,787
    nssv18436691RemappedGoodNC_000022.10:g.269
    58495_26965752del
    GRCh37.p13First PassNC_000022.10Chr2226,958,49526,965,752

    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)
    nssv184366914e-061276258
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