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nsv7030341

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 85 SVs from 23 studies. See in: genome view    
    Submitted genomic26,683,101-26,689,300Question Mark
    Overlapping variant regions from other studies: 85 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):27,079,064-27,085,263Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7030341Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2226,683,10126,689,300
    nsv7030341RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2227,079,06427,085,263

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18436704deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18436704Submitted genomicNC_000022.11:g.266
    83101_26689300del
    GRCh38 (hg38)NC_000022.11Chr2226,683,10126,689,300
    nssv18436704RemappedPerfectNC_000022.10:g.270
    79064_27085263del
    GRCh37.p13First PassNC_000022.10Chr2227,079,06427,085,263

    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)
    nssv18436704<0.00129252300
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