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nsv7059872

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,448,058

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3315 SVs from 79 studies. See in: genome view    
    Submitted genomic3,621,338-5,069,395Question Mark
    Overlapping variant regions from other studies: 3316 SVs from 79 studies. See in: genome view    
    Remapped(Score: Perfect):3,539,379-4,987,436Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059872Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX3,621,3385,069,395
    nsv7059872RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX3,539,3794,987,436

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18657692duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18657692Submitted genomicNC_000023.11:g.362
    1338_5069395dup
    GRCh38 (hg38)NC_000023.11ChrX3,621,3385,069,395
    nssv18657692RemappedPerfectNC_000023.10:g.353
    9379_4987436dup
    GRCh37.p13First PassNC_000023.10ChrX3,539,3794,987,436

    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)
    nssv186576929e-062222222
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