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nsv6933088

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:89,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 363 SVs from 48 studies. See in: genome view    
    Submitted genomic119,989,301-120,078,800Question Mark
    Overlapping variant regions from other studies: 363 SVs from 48 studies. See in: genome view    
    Remapped(Score: Perfect):120,427,105-120,516,604Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6933088Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12119,989,301120,078,800
    nsv6933088RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12120,427,105120,516,604

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18593068duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18593068Submitted genomicNC_000012.12:g.119
    989301_120078800du
    p
    GRCh38 (hg38)NC_000012.12Chr12119,989,301120,078,800
    nssv18593068RemappedPerfectNC_000012.11:g.120
    427105_120516604du
    p
    GRCh37.p13First PassNC_000012.11Chr12120,427,105120,516,604

    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)
    nssv185930684e-061275840
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