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nsv7022562

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26,056

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 159 SVs from 37 studies. See in: genome view    
    Submitted genomic30,471,028-30,497,083Question Mark
    Overlapping variant regions from other studies: 159 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):30,867,015-30,893,070Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7022562Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2230,471,02830,497,083
    nsv7022562RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2230,867,01530,893,070

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18436750deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18436750Submitted genomicNC_000022.11:g.304
    71028_30497083del
    GRCh38 (hg38)NC_000022.11Chr2230,471,02830,497,083
    nssv18436750RemappedPerfectNC_000022.10:g.308
    67015_30893070del
    GRCh37.p13First PassNC_000022.10Chr2230,867,01530,893,070

    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)
    nssv184367508.2e-0523276158
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