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nsv6856577

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:180

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 127 SVs from 24 studies. See in: genome view    
    Submitted genomic66,880,799-66,880,978Question Mark
    Overlapping variant regions from other studies: 127 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):67,793,034-67,793,213Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6856577Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr866,880,79966,880,978
    nsv6856577RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr867,793,03467,793,213

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18741072duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18741072Submitted genomicNC_000008.11:g.668
    80799_66880978dup
    GRCh38 (hg38)NC_000008.11Chr866,880,79966,880,978
    nssv18741072RemappedPerfectNC_000008.10:g.677
    93034_67793213dup
    GRCh37.p13First PassNC_000008.10Chr867,793,03467,793,213

    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)
    nssv187410724e-061232166
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