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nsv7090591

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:670,199

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1246 SVs from 60 studies. See in: genome view    
    Submitted genomic103,123,688-103,793,886Question Mark
    Overlapping variant regions from other studies: 1248 SVs from 60 studies. See in: genome view    
    Remapped(Score: Perfect):102,378,616-103,048,815Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7090591Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX103,123,688103,793,886
    nsv7090591RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX102,378,616103,048,815

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18652692duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18652692Submitted genomicNC_000023.11:g.103
    123688_103793886du
    p
    GRCh38 (hg38)NC_000023.11ChrX103,123,688103,793,886
    nssv18652692RemappedPerfectNC_000023.10:g.102
    378616_103048815du
    p
    GRCh37.p13First PassNC_000023.10ChrX102,378,616103,048,815

    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)
    nssv186526925e-061200000
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