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nsv6936969

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25,163

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 210 SVs from 46 studies. See in: genome view    
    Submitted genomic127,930,438-127,955,600Question Mark
    Overlapping variant regions from other studies: 210 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):128,414,983-128,440,145Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6936969Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12127,930,438127,955,600
    nsv6936969RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12128,414,983128,440,145

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18594067duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18594067Submitted genomicNC_000012.12:g.127
    930438_127955600du
    p
    GRCh38 (hg38)NC_000012.12Chr12127,930,438127,955,600
    nssv18594067RemappedPerfectNC_000012.11:g.128
    414983_128440145du
    p
    GRCh37.p13First PassNC_000012.11Chr12128,414,983128,440,145

    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)
    nssv185940674e-061275900
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