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nsv6780128

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:319,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1060 SVs from 68 studies. See in: genome view    
    Submitted genomic134,610,201-134,929,900Question Mark
    Overlapping variant regions from other studies: 1060 SVs from 68 studies. See in: genome view    
    Remapped(Score: Perfect):133,945,891-134,265,590Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6780128Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5134,610,201134,929,900
    nsv6780128RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5133,945,891134,265,590

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18699523duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18699523Submitted genomicNC_000005.10:g.134
    610201_134929900du
    p
    GRCh38 (hg38)NC_000005.10Chr5134,610,201134,929,900
    nssv18699523RemappedPerfectNC_000005.9:g.1339
    45891_134265590dup
    GRCh37.p13First PassNC_000005.9Chr5133,945,891134,265,590

    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)
    nssv18699523<0.00141271546
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