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nsv6930427

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 218 SVs from 33 studies. See in: genome view    
    Submitted genomic119,988,201-119,989,800Question Mark
    Overlapping variant regions from other studies: 218 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):120,426,005-120,427,604Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6930427Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12119,988,201119,989,800
    nsv6930427RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12120,426,005120,427,604

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18593067duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18593067Submitted genomicNC_000012.12:g.119
    988201_119989800du
    p
    GRCh38 (hg38)NC_000012.12Chr12119,988,201119,989,800
    nssv18593067RemappedPerfectNC_000012.11:g.120
    426005_120427604du
    p
    GRCh37.p13First PassNC_000012.11Chr12120,426,005120,427,604

    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)
    nssv185930675.2e-0514265174
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