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nsv7090477

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,641,775

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2056 SVs from 70 studies. See in: genome view    
    Submitted genomic101,314,695-102,956,469Question Mark
    Overlapping variant regions from other studies: 2062 SVs from 70 studies. See in: genome view    
    Remapped(Score: Good):100,569,683-102,211,397Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7090477Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX101,314,695102,956,469
    nsv7090477RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX100,569,683102,211,397

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18457122deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18457122Submitted genomicNC_000023.11:g.101
    314695_102956469de
    l
    GRCh38 (hg38)NC_000023.11ChrX101,314,695102,956,469
    nssv18457122RemappedGoodNC_000023.10:g.100
    569683_102211397de
    l
    GRCh37.p13First PassNC_000023.10ChrX100,569,683102,211,397

    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)
    nssv184571225e-061200000
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