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nsv7083704

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:765,317

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1229 SVs from 61 studies. See in: genome view    
    Submitted genomic130,399,183-131,164,499Question Mark
    Overlapping variant regions from other studies: 1229 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):129,533,157-130,298,473Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7083704Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX130,399,183131,164,499
    nsv7083704RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX129,533,157130,298,473

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18652981duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18652981Submitted genomicNC_000023.11:g.130
    399183_131164499du
    p
    GRCh38 (hg38)NC_000023.11ChrX130,399,183131,164,499
    nssv18652981RemappedPerfectNC_000023.10:g.129
    533157_130298473du
    p
    GRCh37.p13First PassNC_000023.10ChrX129,533,157130,298,473

    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)
    nssv186529815e-061200000
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