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nsv7080438

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:141,484

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 583 SVs from 53 studies. See in: genome view    
    Submitted genomic22,915,289-23,056,772Question Mark
    Overlapping variant regions from other studies: 584 SVs from 53 studies. See in: genome view    
    Remapped(Score: Perfect):22,933,406-23,074,889Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7080438Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX22,915,28923,056,772
    nsv7080438RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX22,933,40623,074,889

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18459710deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18459710Submitted genomicNC_000023.11:g.229
    15289_23056772del
    GRCh38 (hg38)NC_000023.11ChrX22,915,28923,056,772
    nssv18459710RemappedPerfectNC_000023.10:g.229
    33406_23074889del
    GRCh37.p13First PassNC_000023.10ChrX22,933,40623,074,889

    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)
    nssv184597105e-061200000
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