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nsv7035080

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:319

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 97 SVs from 18 studies. See in: genome view    
    Submitted genomic47,602,751-47,603,069Question Mark
    Overlapping variant regions from other studies: 97 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):46,231,495-46,231,813Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7035080Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2047,602,75147,603,069
    nsv7035080RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2046,231,49546,231,813

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18641511duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18641511Submitted genomicNC_000020.11:g.476
    02751_47603069dup
    GRCh38 (hg38)NC_000020.11Chr2047,602,75147,603,069
    nssv18641511RemappedPerfectNC_000020.10:g.462
    31495_46231813dup
    GRCh37.p13First PassNC_000020.10Chr2046,231,49546,231,813

    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)
    nssv186415114e-061235156
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