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nsv6775057

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:577,188

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2174 SVs from 96 studies. See in: genome view    
    Submitted genomic105,121,090-105,698,277Question Mark
    Overlapping variant regions from other studies: 2174 SVs from 96 studies. See in: genome view    
    Remapped(Score: Perfect):104,456,791-105,033,978Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6775057Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5105,121,090105,698,277
    nsv6775057RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5104,456,791105,033,978

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18696910duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18696910Submitted genomicNC_000005.10:g.105
    121090_105698277du
    p
    GRCh38 (hg38)NC_000005.10Chr5105,121,090105,698,277
    nssv18696910RemappedPerfectNC_000005.9:g.1044
    56791_105033978dup
    GRCh37.p13First PassNC_000005.9Chr5104,456,791105,033,978

    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)
    nssv186969101.5e-054266852
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