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nsv7092254

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:36,931

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 279 SVs from 29 studies. See in: genome view    
    Submitted genomic64,411,180-64,448,110Question Mark
    Overlapping variant regions from other studies: 279 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):63,631,060-63,667,990Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7092254Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX64,411,18064,448,110
    nsv7092254RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX63,631,06063,667,990

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18657114duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18657114Submitted genomicNC_000023.11:g.644
    11180_64448110dup
    GRCh38 (hg38)NC_000023.11ChrX64,411,18064,448,110
    nssv18657114RemappedPerfectNC_000023.10:g.636
    31060_63667990dup
    GRCh37.p13First PassNC_000023.10ChrX63,631,06063,667,990

    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)
    nssv186571142.3e-055217391
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