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nsv7038811

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:210,666

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 514 SVs from 51 studies. See in: genome view    
    Submitted genomic134,679,232-134,889,897Question Mark
    Overlapping variant regions from other studies: 514 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):133,813,262-134,023,927Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7038811Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX134,679,232134,889,897
    nsv7038811RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX133,813,262134,023,927

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765527inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765527Submitted genomicNC_000023.11:g.134
    679232_134889897in
    v
    GRCh38 (hg38)NC_000023.11ChrX134,679,232134,889,897
    nssv18765527RemappedPerfectNC_000023.10:g.133
    813262_134023927in
    v
    GRCh37.p13First PassNC_000023.10ChrX133,813,262134,023,927

    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)
    nssv187655275e-061200000
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