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nsv7079616

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:528,148

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 730 SVs from 56 studies. See in: genome view    
    Submitted genomic152,264,528-152,792,675Question Mark
    Overlapping variant regions from other studies: 540 SVs from 48 studies. See in: genome view    
    Remapped(Score: Pass):151,433,000-151,734,489Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7079616Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX152,264,528152,792,675
    nsv7079616RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX151,433,000151,734,489

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18654527duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18654527Submitted genomicNC_000023.11:g.152
    264528_152792675du
    p
    GRCh38 (hg38)NC_000023.11ChrX152,264,528152,792,675
    nssv18654527RemappedPassNC_000023.10:g.151
    433000_151734489du
    p
    GRCh37.p13First PassNC_000023.10ChrX151,433,000151,734,489

    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)
    nssv186545275e-061200000
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