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nsv6954492

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:80

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 239 SVs from 35 studies. See in: genome view    
    Submitted genomic110,647,684-110,647,763Question Mark
    Overlapping variant regions from other studies: 239 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):111,300,031-111,300,110Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6954492Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr13110,647,684110,647,763
    nsv6954492RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr13111,300,031111,300,110

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18602598duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18602598Submitted genomicNC_000013.11:g.110
    647684_110647763du
    p
    GRCh38 (hg38)NC_000013.11Chr13110,647,684110,647,763
    nssv18602598RemappedPerfectNC_000013.10:g.111
    300031_111300110du
    p
    GRCh37.p13First PassNC_000013.10Chr13111,300,031111,300,110

    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)
    nssv186025980.2753103200360
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