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nsv7030680

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,624

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 287 SVs from 46 studies. See in: genome view    
    Submitted genomic42,890,891-42,898,514Question Mark
    Overlapping variant regions from other studies: 288 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):44,311,001-44,318,624Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7030680Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2142,890,89142,898,514
    nsv7030680RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2144,311,00144,318,624

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18436441deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18436441Submitted genomicNC_000021.9:g.4289
    0891_42898514del
    GRCh38 (hg38)NC_000021.9Chr2142,890,89142,898,514
    nssv18436441RemappedPerfectNC_000021.8:g.4431
    1001_44318624del
    GRCh37.p13First PassNC_000021.8Chr2144,311,00144,318,624

    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)
    nssv184364411.1e-053273326
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