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nsv7006475

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,769

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 27 studies. See in: genome view    
    Submitted genomic2,789,947-2,796,715Question Mark
    Overlapping variant regions from other studies: 99 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):2,770,593-2,777,361Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7006475Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr202,789,9472,796,715
    nsv7006475RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr202,770,5932,777,361

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18431123deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18431123Submitted genomicNC_000020.11:g.278
    9947_2796715del
    GRCh38 (hg38)NC_000020.11Chr202,789,9472,796,715
    nssv18431123RemappedPerfectNC_000020.10:g.277
    0593_2777361del
    GRCh37.p13First PassNC_000020.10Chr202,770,5932,777,361

    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)
    nssv184311234e-061276246
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