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nsv6791446

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:569

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 140 SVs from 24 studies. See in: genome view    
    Submitted genomic26,162,361-26,162,929Question Mark
    Overlapping variant regions from other studies: 140 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):26,162,589-26,163,157Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6791446Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr626,162,36126,162,929
    nsv6791446RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr626,162,58926,163,157

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18714055duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18714055Submitted genomicNC_000006.12:g.261
    62361_26162929dup
    GRCh38 (hg38)NC_000006.12Chr626,162,36126,162,929
    nssv18714055RemappedPerfectNC_000006.11:g.261
    62589_26163157dup
    GRCh37.p13First PassNC_000006.11Chr626,162,58926,163,157

    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)
    nssv187140554e-061250818
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