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nsv7086086

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:956,934

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1305 SVs from 57 studies. See in: genome view    
    Submitted genomic19,521,108-20,478,041Question Mark
    Overlapping variant regions from other studies: 1306 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):19,539,226-20,496,159Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7086086Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX19,521,10820,478,041
    nsv7086086RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX19,539,22620,496,159

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18656660duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18656660Submitted genomicNC_000023.11:g.195
    21108_20478041dup
    GRCh38 (hg38)NC_000023.11ChrX19,521,10820,478,041
    nssv18656660RemappedPerfectNC_000023.10:g.195
    39226_20496159dup
    GRCh37.p13First PassNC_000023.10ChrX19,539,22620,496,159

    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)
    nssv186566605e-061200000
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