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nsv7089507

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:794,660

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1229 SVs from 64 studies. See in: genome view    
    Submitted genomic81,045,335-81,839,994Question Mark
    Overlapping variant regions from other studies: 1229 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):80,300,834-81,095,493Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7089507Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX81,045,33581,839,994
    nsv7089507RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX80,300,83481,095,493

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18657883duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18657883Submitted genomicNC_000023.11:g.810
    45335_81839994dup
    GRCh38 (hg38)NC_000023.11ChrX81,045,33581,839,994
    nssv18657883RemappedPerfectNC_000023.10:g.803
    00834_81095493dup
    GRCh37.p13First PassNC_000023.10ChrX80,300,83481,095,493

    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)
    nssv186578835e-061200000
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