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nsv7081232

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:360,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 879 SVs from 69 studies. See in: genome view    
    Submitted genomic56,736,301-57,097,000Question Mark
    Overlapping variant regions from other studies: 879 SVs from 69 studies. See in: genome view    
    Remapped(Score: Perfect):56,762,734-57,123,433Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7081232Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX56,736,30157,097,000
    nsv7081232RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX56,762,73457,123,433

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18657043duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18657043Submitted genomicNC_000023.11:g.567
    36301_57097000dup
    GRCh38 (hg38)NC_000023.11ChrX56,736,30157,097,000
    nssv18657043RemappedPerfectNC_000023.10:g.567
    62734_57123433dup
    GRCh37.p13First PassNC_000023.10ChrX56,762,73457,123,433

    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)
    nssv186570435e-061200000
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