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nsv7018731

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:171

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 137 SVs from 21 studies. See in: genome view    
    Submitted genomic29,052,744-29,052,914Question Mark
    Overlapping variant regions from other studies: 137 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):30,425,065-30,425,235Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7018731Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2129,052,74429,052,914
    nsv7018731RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2130,425,06530,425,235

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18647226duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18647226Submitted genomicNC_000021.9:g.2905
    2744_29052914dup
    GRCh38 (hg38)NC_000021.9Chr2129,052,74429,052,914
    nssv18647226RemappedPerfectNC_000021.8:g.3042
    5065_30425235dup
    GRCh37.p13First PassNC_000021.8Chr2130,425,06530,425,235

    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)
    nssv186472264e-061233744
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