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nsv7028519

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:198

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 113 SVs from 18 studies. See in: genome view    
    Submitted genomic31,720,570-31,720,767Question Mark
    Overlapping variant regions from other studies: 113 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):30,308,373-30,308,570Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7028519Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2031,720,57031,720,767
    nsv7028519RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2030,308,37330,308,570

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18643534duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18643534Submitted genomicNC_000020.11:g.317
    20570_31720767dup
    GRCh38 (hg38)NC_000020.11Chr2031,720,57031,720,767
    nssv18643534RemappedPerfectNC_000020.10:g.303
    08373_30308570dup
    GRCh37.p13First PassNC_000020.10Chr2030,308,37330,308,570

    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)
    nssv186435344e-061235720
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