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nsv6791799

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:195

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 107 SVs from 17 studies. See in: genome view    
    Submitted genomic11,214,195-11,214,389Question Mark
    Overlapping variant regions from other studies: 107 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):11,214,428-11,214,622Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6791799Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr611,214,19511,214,389
    nsv6791799RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr611,214,42811,214,622

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18709528duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18709528Submitted genomicNC_000006.12:g.112
    14195_11214389dup
    GRCh38 (hg38)NC_000006.12Chr611,214,19511,214,389
    nssv18709528RemappedPerfectNC_000006.11:g.112
    14428_11214622dup
    GRCh37.p13First PassNC_000006.11Chr611,214,42811,214,622

    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)
    nssv187095284e-059222164
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