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nsv7059110

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,695

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 453 SVs from 46 studies. See in: genome view    
    Submitted genomic3,685,074-3,703,768Question Mark
    Overlapping variant regions from other studies: 454 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):3,603,115-3,621,809Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059110Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX3,685,0743,703,768
    nsv7059110RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX3,603,1153,621,809

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18455599deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18455599Submitted genomicNC_000023.11:g.368
    5074_3703768del
    GRCh38 (hg38)NC_000023.11ChrX3,685,0743,703,768
    nssv18455599RemappedPerfectNC_000023.10:g.360
    3115_3621809del
    GRCh37.p13First PassNC_000023.10ChrX3,603,1153,621,809

    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)
    nssv184555991.4e-053214286
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