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nsv7026559

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:974

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 145 SVs from 22 studies. See in: genome view    
    Submitted genomic34,415,289-34,416,262Question Mark
    Overlapping variant regions from other studies: 145 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):33,003,095-33,004,068Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7026559Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2034,415,28934,416,262
    nsv7026559RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2033,003,09533,004,068

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18431361deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18431361Submitted genomicNC_000020.11:g.344
    15289_34416262del
    GRCh38 (hg38)NC_000020.11Chr2034,415,28934,416,262
    nssv18431361RemappedPerfectNC_000020.10:g.330
    03095_33004068del
    GRCh37.p13First PassNC_000020.10Chr2033,003,09533,004,068

    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)
    nssv18431361<0.001202274166
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