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nsv6780491

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:578

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 116 SVs from 20 studies. See in: genome view    
    Submitted genomic11,374,066-11,374,643Question Mark
    Overlapping variant regions from other studies: 116 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):11,374,299-11,374,876Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6780491Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr611,374,06611,374,643
    nsv6780491RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr611,374,29911,374,876

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18709653duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18709653Submitted genomicNC_000006.12:g.113
    74066_11374643dup
    GRCh38 (hg38)NC_000006.12Chr611,374,06611,374,643
    nssv18709653RemappedPerfectNC_000006.11:g.113
    74299_11374876dup
    GRCh37.p13First PassNC_000006.11Chr611,374,29911,374,876

    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)
    nssv187096538e-062251154
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