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nsv7086544

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,973

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 274 SVs from 22 studies. See in: genome view    
    Submitted genomic27,800,507-27,806,479Question Mark
    Overlapping variant regions from other studies: 275 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):27,818,624-27,824,596Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7086544Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX27,800,50727,806,479
    nsv7086544RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX27,818,62427,824,596

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18452662deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18452662Submitted genomicNC_000023.11:g.278
    00507_27806479del
    GRCh38 (hg38)NC_000023.11ChrX27,800,50727,806,479
    nssv18452662RemappedPerfectNC_000023.10:g.278
    18624_27824596del
    GRCh37.p13First PassNC_000023.10ChrX27,818,62427,824,596

    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)
    nssv184526625e-061200000
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