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nsv7036676

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:58

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 80 SVs from 20 studies. See in: genome view    
    Submitted genomic40,405,313-40,405,370Question Mark
    Overlapping variant regions from other studies: 80 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):40,801,317-40,801,374Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7036676Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2240,405,31340,405,370
    nsv7036676RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2240,801,31740,801,374

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18453892deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18453892Submitted genomicNC_000022.11:g.404
    05313_40405370del
    GRCh38 (hg38)NC_000022.11Chr2240,405,31340,405,370
    nssv18453892RemappedPerfectNC_000022.10:g.408
    01317_40801374del
    GRCh37.p13First PassNC_000022.10Chr2240,801,31740,801,374

    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)
    nssv18453892<0.00146249996
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